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Article

The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.

Genomics - 1 Jul 1991

Travis G H, Christerson L, Danielson P E, Klisak I, Sparkes R S, Hahn L B, Dryja T P, Sutcliffe J G

Abstract excerpt

Retinal degeneration slow (rds) is a mouse neurological mutation that is characterized phenotypically by abnormal development of rod and cone photoreceptors followed by their slow degeneration. This phenotype resembles the pathologic abnormalities seen in retinitis pigmentosa. The mouse rds gene has recently been cloned. Here we present the sequence of a full-length cDNA clone of the human RDS mRNA. We show that...

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PMID: 1679750
DOI: 10.1016/0888-7543(91)90457-p

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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.

Related research

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The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.PMID 1679750Read ↗

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Photoreceptor-specific mRNAs in mice carrying different allelic combinations at the rd and rds loci.Semantic proximity Read ↗

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Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions.Semantic proximity Read ↗

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the <i>rd7</i> mouseSemantic proximity Read ↗

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