Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.

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Article

Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.

Investigative ophthalmology & visual science - 1 Mar 1998

Sippel K C, DeStefano J D, Berson E L, Dryja T P

Abstract excerpt

PURPOSE: To establish the DNA sequence of the coding regions of the human arrestin locus and to determine whether defects in this sequence are present among patients with retinitis pigmentosa (RP) or types of stationary night blindness in addition to Oguchi disease. METHODS: The human genomic loc...

Topics

Arrestin
Cloning, Molecular
DNA Primers
Exons
Female
Humans
Introns
Male
Mutation
Night Blindness
Pedigree
Polymorphism, Single-Stranded Conformational
Retinitis Pigmentosa
Sequence Analysis, DNA

Source

Open in PubMed

Identifiers

PMID: 9501883

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9501883-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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