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	581.	New mutations in the PLEC gene in a Chinese patient with epidermolysis bullosa simplex with muscular dystrophy. [electronic resource] by Chen, Q Lin, Z M Wang, H J Zhang, J Yin, J H Yang, Y Producer: 20140530 In: Clinical and experimental dermatology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	582.	Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients. [electronic resource] by Amr, Khalda Messaoud, Olfa El Darouti, Mohamad Abdelhak, Sonia El-Kamah, Ghada Producer: 20140121 In: Gene vol. 533 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	583.	Factor V deficiency caused by a novel nonsense mutation (Gln2031stop) in a Chinese patient. [electronic resource] by Wang, Yingyu Zhu, Liqing Ye, Lianmin Xie, Yaosheng Pan, Jingye Wang, Mingshan Producer: 20150113 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	584.	A novel silent deletion, an insertion mutation and a nonsense mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome. [electronic resource] by Wang, Yan Yin, Xiao-Juan Han, Tao Peng, Wei Wu, Hong-Lin Liu, Xin Feng, Zhi-Chun Producer: 20150121 In: Molecular genetics and genomics : MGG vol. 289 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	585.	A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis Bullosa. [electronic resource] by Rotemberg, Veronica Garzon, Maria Lauren, Christine Iglesias, Alejandro Brachio, Sandhya S Aggarwal, Vimla Stong, Nicholas Goldstein, David B Diacovo, Thomas Producer: 20171211 In: The Journal of pediatrics vol. 191 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	586.	A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy. [electronic resource] by Zambonin, J L Dyment, D A Xi, Y Lamont, R E Hartley, T Miller, E Kerr, M Boycott, K M Parboosingh, J S Venkateswaran, S Producer: 20191003 In: Neurogenetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	587.	Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development. [electronic resource] by Chen, C Xu, X Kong, L Li, P Zhou, F Zhao, S Xin, X Tan, J Zhang, X Producer: 20190401 In: Human reproduction (Oxford, England) vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	588.	[Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene]. [electronic resource] by Liu, Hongyan Huang, Jia Jiang, Yinghai Guo, Liangjie Xiao, Hai Wang, Hongdan Producer: 20200113 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	589.	Inhibitory regulation of calcium transients in prefrontal dendritic spines is compromised by a nonsense Shank3 mutation. [electronic resource] by Ali, Farhan Shao, Ling-Xiao Gerhard, Danielle M Sweasy, Katherine Pothula, Santosh Pittenger, Christopher Duman, Ronald S Kwan, Alex C Producer: 20211011 In: Molecular psychiatry vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	590.	Two novel LDL receptor mutations in familial hypercholesterolemia: C122Y and E296X. [electronic resource] by Genschel, J Thomas, H P Kassner, U Lochs, H Steinhagen-Thiessen, E Schmidt, H H Producer: 20010816 In: Human mutation vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	591.	Nonsense mutations in a Becker muscular dystrophy and an intermediate patient. [electronic resource] by Prior, T W Bartolo, C Papp, A C Snyder, P J Sedra, M S Burghes, A H Mendell, J R Producer: 19960806 In: Human mutation vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	592.	Gene symbol: ALAS2. Disease: sideroblastic anaemia. [electronic resource] by Pereira, J C Gonçalves, P Cuhna, E Ribeiro, M L Producer: 20050223 In: Human genetics vol. 115 Availability: No items available. Save to lists Add to cart (remove)
	593.	pho2, a phosphate overaccumulator, is caused by a nonsense mutation in a microRNA399 target gene. [electronic resource] by Aung, Kyaw Lin, Shu-I Wu, Chia-Chune Huang, Yu-Ting Su, Chun-Lin Chiou, Tzyy-Jen Producer: 20061114 In: Plant physiology vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	594.	RNA stability: is it the endo' the world as we know it? [electronic resource] by Wilusz, Jeffrey Producer: 20090129 In: Nature structural & molecular biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	595.	A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures. [electronic resource] by Gallanti, Andrea Tonelli, Alessandra Cardin, Veronica Bussone, Gennaro Bresolin, Nereo Bassi, Maria Teresa Producer: 20090206 In: Journal of the neurological sciences vol. 273 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	596.	Gene symbol: MTM1. Disease: Myotubular myopathy? [electronic resource] by Mueller, O Thomas Coovadia, Adam Producer: 20101124 In: Human genetics vol. 123 Availability: No items available. Save to lists Add to cart (remove)
	597.	Unassigned codons, nonsense suppression, and anticodon modifications in the evolution of the genetic code. [electronic resource] by van der Gulik, Peter T S Hoff, Wouter D Producer: 20120409 In: Journal of molecular evolution vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	598.	Two novel patients with Bohring-Opitz syndrome caused by de novo ASXL1 mutations. [electronic resource] by Magini, Pamela Della Monica, Matteo Uzielli, Maria Luisa Giovannucci Mongelli, Patrizia Scarselli, Gloria Gambineri, Eleonora Scarano, Gioacchino Seri, Marco Producer: 20120730 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	599.	A MYB transcription factor controls flower color in soybean. [electronic resource] by Takahashi, Ryoji Yamagishi, Noriko Yoshikawa, Nobuyuki Producer: 20130605 In: The Journal of heredity vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	600.	Rice dwarf viruses with dysfunctional genomes generated in plants are filtered out in vector insects: implications for the origin of the virus. [electronic resource] by Pu, Yingying Kikuchi, Akira Moriyasu, Yusuke Tomaru, Masatoshi Jin, Yan Suga, Haruhisa Hagiwara, Kyoji Akita, Fusamichi Shimizu, Takumi Netsu, Osamu Suzuki, Nobuhiro Uehara-Ichiki, Tamaki Sasaya, Takahide Wei, Taiyun Li, Yi Omura, Toshihiro Producer: 20110411 In: Journal of virology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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