Elovl4 haploinsufficiency does not induce early onset retinal degeneration in mice

ELOVL4 was first identified as a disease-causing gene in Stargardt macular dystrophy (STGD3, MIM 600110.) To date, three ELOVL4 mutations have been identified, all of which result in truncated proteins which induce autosomal dominant juvenile macular degenerations. Based on sequence homology, ELOVL4...

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Detalhes bibliográficos
Main Authors: Li, Wenmei, Chen, Yali, Cameron, D. Joshua, Wang, Changguan, Karan, Goutam, Yang, Zhenglin, Zhao, Yu, Pearson, Erik, Chen, Haoyu, Deng, Chuxia, Howes, Kimberly, Zhang, Kang
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2583245/
https://ncbi.nlm.nih.gov/pubmed/17254625
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.visres.2006.10.023
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