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Article

Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.

Genomics - 1 Feb 1992

Bech-Hansen N T, Moore B J, Pearce W G

Abstract excerpt

A recombinant chromosome in a male affected with X-linked congenital stationary night blindness (CSNB1) provides new information on the location of the CSNB1 locus. A four-generation family with five males affected with X-linked CSNB was analyzed with five polymorphic markers for four X-chromosome loci spanning the region OTC (Xp21.1) to DXS255 (Xp11.22). Four of the males inherited the same X chromosome; one...

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Source

Identifiers

PMID: 1740347
DOI: 10.1016/0888-7543(92)90394-8

Genes

OTC

Provenance

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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Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.PMID 1740347Read ↗

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