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	381.	MC1R studies in dogs with melanistic mask or brindle patterns. [electronic resource] by Schmutz, S M Berryere, T G Ellinwood, N M Kerns, J A Barsh, G S Producer: 20031210 In: The Journal of heredity vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	382.	A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner. [electronic resource] by Lanschuetzer, C M Klausegger, A Pohla-Gubo, G Hametner, R Richard, G Uitto, J Hintner, H Bauer, J W Producer: 20030425 In: Clinical and experimental dermatology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	383.	Nonsense mutation in the ALOX12B gene leads to autosomal recessive congenital ichthyosis in a Lebanese family. [electronic resource] by Kurban, M Shimomura, Y Bahhady, R Ghosn, S Kibbi, A-G Christiano, A M Producer: 20100601 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	384.	Adenovirus serotype 5 L4-22K and L4-33K proteins have distinct functions in regulating late gene expression. [electronic resource] by Morris, Susan J Leppard, Keith N Producer: 20090330 In: Journal of virology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	385.	Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria. [electronic resource] by Murata, Ichidai Hozumi, Yutaka Kawaguchi, Masakazu Katagiri, Yoshiyuki Yasumoto, Shinichiro Kubo, Yoshiaki Fujimoto, Wataru Horikawa, Tatsuya Kondo, Taisuke Kono, Michihiro Tomita, Yasushi Suzuki, Tamio Producer: 20090305 In: Journal of dermatological science vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	386.	Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions. [electronic resource] by Ashoor, Ghalia G Greenstein, Robert M Lam, Hamut Martinez-Mir, Amalia Zlotogorski, Abraham Christiano, Angela M Producer: 20051110 In: Journal of dermatological science vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	387.	A homozygous nonsense mutation in the EVER2 gene leads to epidermodysplasia verruciformis. [electronic resource] by Sun, X-K Chen, J-F Xu, A-E Producer: 20051121 In: Clinical and experimental dermatology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	388.	[Epidermolysis bullosa simplex]. [electronic resource] by Dereure, O Producer: 20060428 In: Annales de dermatologie et de venereologie vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	389.	Gene symbol: ARSA. Disease: metachromatic leukodystrophy. [electronic resource] by Berna, L Gieselmann, V Poupetova, H Hrebicek, M Elleder, M Ledvinova, J Producer: 20060321 In: Human genetics vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	390.	Gene symbol: f9. [electronic resource] by Niceta, Marcello Carmelo, Fabiano Pietro, Sammarco Fabio, Gagliano Giacomo, Mancuso Producer: 20070720 In: Human genetics vol. 121 Availability: No items available. Save to lists Add to cart (remove)
	391.	Messenger RNA surveillance systems monitoring proper translation termination. [electronic resource] by Akimitsu, Nobuyoshi Producer: 20080701 In: Journal of biochemistry vol. 143 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	392.	Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene. [electronic resource] by Priore Oliva, C Carubbi, F Schaap, F G Bertolini, S Calandra, S Producer: 20080409 In: Journal of internal medicine vol. 263 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	393.	Amber mutants of bacteriophage T4D: their isolation and genetic characterization. [electronic resource] by Epstein, Richard H Bolle, Antoinette Steinberg, Charles M Producer: 20120803 In: Genetics vol. 190 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	394.	Novel human pathological mutations. Gene symbol: Zmpste24. Disease: Restrictive dermopathy. [electronic resource] by Saxena, Renu Kohli, Sudha Verma, I C Producer: 20110506 In: Human genetics vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	395.	Regulation of nonsense-mediated mRNA decay: implications for physiology and disease. [electronic resource] by Karam, Rachid Wengrod, Jordan Gardner, Lawrence B Wilkinson, Miles F Producer: 20130805 In: Biochimica et biophysica acta vol. 1829 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	396.	A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia. [electronic resource] by Marchi, Rita Brennan, Stephen Meyer, Michael Rojas, Héctor Kanzler, Daniela De Agrela, Marisela Ruiz-Saez, Arlette Producer: 20130723 In: Blood cells, molecules & diseases vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	397.	Atopic dermatitis: scratching through the complexity of barrier dysfunction. [electronic resource] by Sprecher, Eli Leung, Donald Y M Producer: 20140107 In: The Journal of allergy and clinical immunology vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	398.	The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603* in a female patient with pachydermoperiostosis with an atypical phenotype. [electronic resource] by Niizeki, H Shiohama, A Sasaki, T Seki, A Kabashima, K Otsuka, A Takeshita, M Hirakiyama, A Okuyama, T Tanese, K Ishiko, A Amagai, M Kudoh, J Producer: 20150112 In: The British journal of dermatology vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	399.	First de novo ANK3 nonsense mutation in a boy with intellectual disability, speech impairment and autistic features. [electronic resource] by Kloth, Katja Denecke, Jonas Hempel, Maja Johannsen, Jessika Strom, Tim M Kubisch, Christian Lessel, Davor Producer: 20171207 In: European journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	400.	Extensive Erythema and Hyperkeratosis on the Extremities and Lumbar Area as an Unusual Mani-festation of Nagashima-type Palmoplantar Keratosis. [electronic resource] by Miyauchi, Toshinari Nomura, Toshifumi Suzuki, Shotaro Ohguchi, Yuka Yamaguchi, Yasuyuki Shinkuma, Satoru Natsuga, Ken Fujita, Yasuyuki Shimizu, Hiroshi Producer: 20170116 In: Acta dermato-venereologica vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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