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	401.	Screening of the epsilon sarcoglycan gene in Tourette syndrome and obsessive compulsive disorder. [electronic resource] by Katerberg, Hilga Cath, Danielle C Tijssen, Marina A J van Balkom, Anton J L M van de Leemput, Yvonne L C den Boer, Johan A Heutink, Peter Baas, Frank Producer: 20080428 In: Psychiatric genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	402.	Dystonia-plus syndromes. [electronic resource] by Asmus, F Gasser, T Producer: 20101101 In: European journal of neurology vol. 17 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	403.	Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia. [electronic resource] by Grütz, Karen Seibler, Philip Weissbach, Anne Lohmann, Katja Carlisle, Francesca A Blake, Derek J Westenberger, Ana Klein, Christine Grünewald, Anne Producer: 20181025 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	404.	Abnormal expression of heparin sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency. [electronic resource] by Higuchi, I Fukunaga, H Matsumura, K Inose, M Izumi, K Okubo, R Nakagawa, M Shimizu, T Osame, M Producer: 19960320 In: Neuromuscular disorders : NMD vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	405.	[Gene therapy--its present status and future direction]. [electronic resource] by Toyooka, T Producer: 20001124 In: Nihon yakurigaku zasshi. Folia pharmacologica Japonica vol. 116 Availability: No items available. Save to lists Add to cart (remove)
	406.	β-Sarcoglycan gene transfer decreases fibrosis and restores force in LGMD2E mice. [electronic resource] by Pozsgai, E R Griffin, D A Heller, K N Mendell, J R Rodino-Klapac, L R Producer: 20161006 In: Gene therapy vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	407.	Sarcoglycan complex in human normal and pathological prostatic tissue: an immunohistochemical and RT-PCR study. [electronic resource] by Cutroneo, Giuseppina Bramanti, Placido Favaloro, Angelo Anastasi, Giuseppe Trimarchi, Fabio Di Mauro, Debora Rinaldi, Carmela Speciale, Francesco Inferrera, Antonino Santoro, Giuseppe Arena, Salvatore Patricolo, Mario Magno, Carlo Producer: 20140915 In: Anatomical record (Hoboken, N.J. : 2007) vol. 297 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	408.	Regulation of the dystrophin-associated glycoprotein complex composition by the metabolic properties of muscle fibres. [electronic resource] by Omairi, Saleh Hau, Kwan-Leong Collins-Hooper, Henry Scott, Charlotte Vaiyapuri, Sakthivel Torelli, Silvia Montanaro, Federica Matsakas, Antonios Patel, Ketan Producer: 20200915 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	409.	epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D. [electronic resource] by Ettinger, A J Feng, G Sanes, J R Producer: 19980122 In: The Journal of biological chemistry vol. 272 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	410.	[Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification]. [electronic resource] by Teijeira-Bautista, S García-García, D Teijeiro-Ferreira, A Fernández-Hojas, R Fernández-Rodríguez, J M Navarro-Fernández-Balbuena, C Producer: 19980908 In: Revista de neurologia vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	411.	High intake of saturated fat, but not polyunsaturated fat, improves survival in heart failure despite persistent mitochondrial defects. [electronic resource] by Galvao, Tatiana F Brown, Bethany H Hecker, Peter A O'Connell, Kelly A O'Shea, Karen M Sabbah, Hani N Rastogi, Sharad Daneault, Caroline Des Rosiers, Christine Stanley, William C Producer: 20120508 In: Cardiovascular research vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	412.	Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities. [electronic resource] by Mora, M Moroni, I Uziel, G di Blasi, C Barresi, R Farina, L Morandi, L Producer: 19970227 In: Neuromuscular disorders : NMD vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	413.	Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. [electronic resource] by Gouveia, Telma L F Paim, Julia F O Pavanello, Rita C Zatz, Mayana Vainzof, Mariz Producer: 20060727 In: Diagnostic molecular pathology : the American journal of surgical pathology, part B vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	414.	Magic-factor 1, a partial agonist of Met, induces muscle hypertrophy by protecting myogenic progenitors from apoptosis. [electronic resource] by Cassano, Marco Biressi, Stefano Finan, Amanda Benedetti, Laura Omes, Claudia Boratto, Renata Martin, Frank Allegretti, Marcello Broccoli, Vania Cusella De Angelis, Gabriella Comoglio, Paolo M Basilico, Cristina Torrente, Yvan Michieli, Paolo Cossu, Giulio Sampaolesi, Maurilio Producer: 20081125 In: PloS one vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	415.	Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. [electronic resource] by Saxena, Richa Saleheen, Danish Been, Latonya F Garavito, Martha L Braun, Timothy Bjonnes, Andrew Young, Robin Ho, Weang Kee Rasheed, Asif Frossard, Philippe Sim, Xueling Hassanali, Neelam Radha, Venkatesan Chidambaram, Manickam Liju, Samuel Rees, Simon D Ng, Daniel Peng-Keat Wong, Tien-Yin Yamauchi, Toshimasa Hara, Kazuo Tanaka, Yasushi Hirose, Hiroshi McCarthy, Mark I Morris, Andrew P Basit, Abdul Barnett, Anthony H Katulanda, Prasad Matthews, David Mohan, Viswanathan Wander, Gurpreet S Singh, Jai Rup Mehra, Narinder K Ralhan, Sarju Kamboh, M Ilyas Mulvihill, John J Maegawa, Hiroshi Tobe, Kazuyuki Maeda, Shiro Cho, Yoon S Tai, E Shyong Kelly, M Ann Chambers, John C Kooner, Jaspal S Kadowaki, Takashi Deloukas, Panos Rader, Daniel J Danesh, John Sanghera, Dharambir K Producer: 20130628 In: Diabetes vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	416.	Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect. [electronic resource] by Mojbafan, Marzieh Bahmani, Reza Bagheri, Samira Dabbagh Sharifi, Zohreh Zeinali, Sirous Producer: 20210201 In: Orphanet journal of rare diseases vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	417.	Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. [electronic resource] by Zimprich, A Grabowski, M Asmus, F Naumann, M Berg, D Bertram, M Scheidtmann, K Kern, P Winkelmann, J Müller-Myhsok, B Riedel, L Bauer, M Müller, T Castro, M Meitinger, T Strom, T M Gasser, T Producer: 20010927 In: Nature genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	418.	Partial loss of NADPH-diaphorase/nitric oxide synthase-complex in amyotrophic lateral sclerosis and human type-II myofiber atrophy. [electronic resource] by Schoser, B G Lück, G Blottner, D Producer: 19980113 In: Neuroscience letters vol. 231 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	419.	Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophies. [electronic resource] by Gazzerro, Elisabetta Assereto, Stefania Bonetto, Andrea Sotgia, Federica Scarfì, Sonia Pistorio, Angela Bonuccelli, Gloria Cilli, Michele Bruno, Claudio Zara, Federico Lisanti, Michael P Minetti, Carlo Producer: 20101214 In: The American journal of pathology vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	420.	Chronic oral administration of Ang-(1-7) improves skeletal muscle, autonomic and locomotor phenotypes in muscular dystrophy. [electronic resource] by Sabharwal, Rasna Cicha, Michael Z Sinisterra, Ruben D M De Sousa, Frederico B Santos, Robson A Chapleau, Mark W Producer: 20140521 In: Clinical science (London, England : 1979) vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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