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	1081.	MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families. [electronic resource] by Braathen, Geir J Sand, Jette C Lobato, Ana Høyer, Helle Russell, Michael B Producer: 20100430 In: BMC medical genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1082.	Seipin S90L mutation in an Italian family with CMT2/dHMN and pyramidal signs. [electronic resource] by Luigetti, M Fabrizi, G M Madia, F Ferrarini, M Conte, A Delgrande, A Tonali, P A Sabatelli, M Producer: 20100916 In: Muscle & nerve vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1083.	Impact of I30T and I30M substitution in MPZ gene associated with Dejerine-Sottas syndrome type B (DSSB): A molecular modeling and dynamics. [electronic resource] by Agrahari, Ashish George Priya Doss, C Producer: 20160523 In: Journal of theoretical biology vol. 382 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1084.	A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. [electronic resource] by Santoro, L Manganelli, F Lanzillo, R Tessa, A Barbieri, F Pierelli, F Di Giacinto, G Nigro, V Santorelli, F M Producer: 20070316 In: Journal of neurology vol. 253 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1085.	Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutation. [electronic resource] by Craig, K Elliott, H R Keers, S M Lambert, C Pyle, A Graves, T D Woodward, C Sweeney, M G Davis, M B Hanna, M G Chinnery, P F Producer: 20080201 In: Journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1086.	Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia. [electronic resource] by Zimoń, Magdalena Baets, Jonathan Almeida-Souza, Leonardo De Vriendt, Els Nikodinovic, Jelena Parman, Yesim Battaloğlu, Esra Matur, Zeliha Guergueltcheva, Velina Tournev, Ivailo Auer-Grumbach, Michaela De Rijk, Peter Petersen, Britt-Sabina Müller, Thomas Fransen, Erik Van Damme, Philip Löscher, Wolfgang N Barišić, Nina Mitrovic, Zoran Previtali, Stefano C Topaloğlu, Haluk Bernert, Günther Beleza-Meireles, Ana Todorovic, Slobodanka Savic-Pavicevic, Dusanka Ishpekova, Boryana Lechner, Silvia Peeters, Kristien Ooms, Tinne Hahn, Angelika F Züchner, Stephan Timmerman, Vincent Van Dijck, Patrick Rasic, Vedrana Milic Janecke, Andreas R De Jonghe, Peter Jordanova, Albena Producer: 20121210 In: Nature genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1087.	Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation. [electronic resource] by Yamashita, Satoshi Kimura, En Zhang, Ziwei Tawara, Nozomu Hara, Kentaro Yoshimura, Akiko Takashima, Hiroshi Ando, Yukio Producer: 20200113 In: Muscle & nerve vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1088.	Magnetic resonance imaging in the malformative syndromes with mental retardation. [electronic resource] by Gabrielli, O Salvolini, U Coppa, G V Catassi, C Rossi, R Manca, A Lanza, R Giorgi, P L Producer: 19910322 In: Pediatric radiology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1089.	Clinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene. [electronic resource] by Tamaru, Y Hirano, M Ito, H Kawamura, J Matsumoto, S Imai, T Ueno, S Producer: 19980514 In: Journal of neurology, neurosurgery, and psychiatry vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1090.	[Hepatomioneuropathy secondary to mitochondrial DNA depletion]. [electronic resource] by Blanco-Barca, M O Gómez-Lado, C Campos-González, Y Castro-Gago, M Producer: 20070614 In: Neurologia (Barcelona, Spain) vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	1091.	Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion. [electronic resource] by Kim, Seung Min Chung, Ki Wha Choi, Byung Ok Yoon, Eui Soo Choi, Jung Young Park, Kee Duk Sunwoo, Il Nam Producer: 20041210 In: Experimental & molecular medicine vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1092.	Vincristine exacerbates asymptomatic Charcot-Marie-tooth disease with a novel EGR2 mutation. [electronic resource] by Nakamura, Tomonori Hashiguchi, Akihiro Suzuki, Shinsuke Uozumi, Kimiharu Tokunaga, Shoko Takashima, Hiroshi Producer: 20120522 In: Neurogenetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1093.	A Case of Apoplexy Attack-Like Neuropathy due to Hereditary Neuropathy with Liability to Pressure Palsies in a Patient Diagnosed with Chronic Cerebral Infarction. [electronic resource] by Hachisuka, Akiko Matsushima, Yasuyuki Hachisuka, Kenji Saeki, Satoru Producer: 20170410 In: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1094.	The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes. [electronic resource] by Inoue, K Dewar, K Katsanis, N Reiter, L T Lander, E S Devon, K L Wyman, D W Lupski, J R Birren, B Producer: 20010920 In: Genome research vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1095.	Rapid detection of duplication/deletion of the PMP22 gene in patients with Charcot-Marie-Tooth disease Type 1A and hereditary neuropathy with liability to pressure palsy by real-time quantitative PCR using SYBR Green I dye. [electronic resource] by Kim, Sang-Wun Lee, Kwang-Soo Jin, Hyun-Seok Lee, Tae-Mi Koo, Soo Kyung Lee, Yong-Jun Jung, Sung-Chul Producer: 20040609 In: Journal of Korean medical science vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1096.	Dysmyelinated lower motor neurons retract and regenerate dysfunctional synaptic terminals. [electronic resource] by Yin, Xinghua Kidd, Grahame J Pioro, Erik P McDonough, Jennifer Dutta, Ranjan Feltri, M Laura Wrabetz, Lawrence Messing, Albee Wyatt, Ryan M Balice-Gordon, Rita J Trapp, Bruce D Producer: 20040721 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1097.	Rapid functional analysis in Xenopus oocytes of Po protein adhesive interactions. [electronic resource] by Yoshida, M Colma, D R Producer: 20020129 In: Neurochemical research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1098.	Androgen receptor mRNA with increased size of tandem CAG repeat is widely expressed in the neural and nonneural tissues of X-linked recessive bulbospinal neuronopathy. [electronic resource] by Doyu, M Sobue, G Kimata, K Yamamoto, K Mitsuma, T Producer: 19950428 In: Journal of the neurological sciences vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1099.	Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele. [electronic resource] by Adlkofer, K Naef, R Suter, U Producer: 19971105 In: Journal of neuroscience research vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1100.	Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine. [electronic resource] by Hryshchenko, N V Livshits, L A Producer: 20091218 In: TSitologiia i genetika vol. 43 Availability: No items available. Save to lists Add to cart (remove)

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