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Article

Identification of the gene and the mutation responsible for the mouse nob phenotype.

Investigative ophthalmology & visual science - 1 Jan 2003

Gregg Ronald G, Mukhopadhyay Suparna, Candille Sophie I, Ball Sherry L, Pardue Machelle T, McCall Maureen A, Peachey Neal S

Abstract excerpt

PURPOSE: The available evidence indicates that the naturally occurring mouse mutant nob (no b-wave) provides an animal model for the complete form of human X-linked congenital stationary night blindness (CSNB1). The goals of the present study were to identify the nob gene defect, to characterize the expression pattern of the involved gene, and to assess visual sensitivity in nob mice. METHODS: Positional cloning,...

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Identifiers

PMID: 12506099
DOI: 10.1167/iovs.02-0501

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification of the gene and the mutation responsible for the mouse nob phenotype.PMID 12506099Read ↗

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The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.Semantic proximity Read ↗

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