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Article

Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21.

American journal of medical genetics - 17 Jan 2000

Ghiasvand N M, Kanis A B, Helms C, Sheffield V C, Stone E M, Donis-Keller H

Abstract excerpt

Nonsyndromic congenital retinal nonattachment (NCRNA) comprises congenital insensitivity to light, massive retrolental mass, shallow anterior chamber, microphthalmia, and nystagmus. We searched for the location of the gene responsible for an autosomal recessive form of NCRNA by using DNA samples from 36 individuals from a founding population. To this end we applied homozygosity mapping and a DNA pooling strategy...

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Identifiers

PMID: 10607958
DOI: 10.1002/(sici)1096-8628(20000117)90:2<165::aid-ajmg15>3.0.co;2-o

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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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