Uncoupling of Photoreceptor Peripherin/rds Fusogenic Activity from Biosynthesis, Subunit Assembly, and Targeting: A POTENTIAL MECHANISM FOR PATHOGENIC EFFECTS

Inherited defects in the RDS gene cause a multiplicity of progressive retinal diseases in humans. The gene product, peripherin/rds (P/rds), is a member of the tetraspanin protein family required for normal vertebrate photoreceptor outer segment (OS) architecture. Although its molecular function rema...

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Hlavní autoři: Ritter, Linda M., Khattree, Nidhi, Chen, Shu-Chu, Goldberg, Andrew F. X., Boesze-Battaglia, Kathleen, Tam, Beatrice M., Moritz, Orson L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2004
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1360210/
https://ncbi.nlm.nih.gov/pubmed/15252042
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M403943200
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