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Article

RDS Functional Domains and Dysfunction in Disease.

Advances in experimental medicine and biology - 1 Jan 2016

Stuck Michael W, Conley Shannon M, Naash Muna I

Abstract excerpt

The photoreceptor specific tetraspanin protein retina degeneration slow (RDS) is a critical component of the machinery necessary for the formation of rod and cone outer segments. Over 80 individual pathogenic mutations in RDS have been identified in human patients that lead to a wide variety of retinal degenerative diseases including retinitis pigmentosa, cone-rod dystrophy, and various forms of macular...

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Share to Genetic Predisposition to Disease
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Protein Multimerization

Share to Protein Structure, Tertiary

Share to Retinitis Pigmentosa

Source

Identifiers

PMID: 26427414
DOI: 10.1007/978-3-319-17121-0_29

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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