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Article

Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome.

Investigative ophthalmology & visual science - 1 Oct 1999

Candille S I, Pardue M T, McCall M A, Peachey N S, Gregg R G

Abstract excerpt

PURPOSE: To determine the position on the X chromosome of the gene responsible for a spontaneous mouse mutation, nob (no b-wave), which matches the phenotype of complete X-linked congenital stationary night blindness (CSNB) type 1 in human. METHODS: Inter- and intraspecific pedigrees were generated, and the phenotype of each mouse was scored on the basis of either the presence or the absence of an...

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PMID: 10509675

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

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