ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement

PURPOSE. Photoreceptor degeneration (PRD) is a genetically heterogeneous retinal disorder. Although a number of genes involved in PRD have been identified, their genetic basis remains unknown in a significant number of patients. In this study, we aimed to identify novel disease-causing genes of PRD....

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Invest Ophthalmol Vis Sci
Hlavní autoři: Xu, Mingchu, Gelowani, Violet, Eblimit, Aiden, Wang, Feng, Young, Marielle P., Sawyer, Briana L., Zhao, Li, Jenkins, Glen, Creel, Donnell J., Wang, Keqing, Ge, Zhongqi, Wang, Hui, Li, Yumei, Hartnett, M. Elizabeth, Chen, Rui
Médium: Artigo
Jazyk:Inglês
Vydáno: The Association for Research in Vision and Ophthalmology 2015
Témata:
Genetics
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4468593/
https://ncbi.nlm.nih.gov/pubmed/26070061
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.15-16778
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky