REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking

Author:

Agrawal Smriti A.,Burgoyne Thomas,Eblimit Aiden,Bellingham James,Parfitt David A.,Lane Amelia,Nichols Ralph,Asomugha Chinwe,Hayes Matthew J.,Munro Peter M.,Xu Mingchu,Wang Keqing,Futter Clare E.,Li Yumei,Chen Rui,Cheetham Michael E.

Funder

Foundation Fighting Blindness

National Eye Institute

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference50 articles.

1. Genetics in retinal diseases;Riaz;Dev. Ophthalmol,2016

2. Retinal dystrophies, genomic applications in diagnosis and prospects for therapy;Nash;Transl. Pediatr,2015

3. Genes and mutations causing autosomal dominant retinitis pigmentosa;Daiger;Clin. Genet,2014

4. Contributions of genetics to our understanding of inherited monogenic retinal diseases and age-related macular degeneration;Bok;Arch. Ophthalmol,2007

5. Aberrant protein trafficking in retinal degenerations: The initial phase of retinal remodeling;Bales;Exp. Eye Res,2016

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