Usherin defects lead to early-onset retinal dysfunction in zebrafish

Mutations in USH2A are the most frequent cause of Usher syndrome and autosomal recessive nonsyndromic retinitis pigmentosa. To unravel the pathogenic mechanisms underlying USH2A-associated retinal degeneration and to evaluate future therapeutic strategies that could potentially halt the progression...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Exp Eye Res
Prif Awduron: Dona, Margo, Slijkerman, Ralph, Lerner, Kimberly, Broekman, Sanne, Wegner, Jeremy, Howat, Taylor, Peters, Theo, Hetterschijt, Lisette, Boon, Nando, de Vrieze, Erik, Sorusch, Nasrin, Wolfrum, Uwe, Kremer, Hannie, Neuhauss, Stephan, Zang, Jingjing, Kamermans, Maarten, Westerfield, Monte, Phillips, Jennifer, van Wijk, Erwin
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2018
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6054812/
https://ncbi.nlm.nih.gov/pubmed/29777677
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2018.05.015
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