Cargando...
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...
Gardado en:
Publicado en: | Exp Eye Res |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado: |
2018
|
Assuntos: | |
Acceso en liña: | 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 |
Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|