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Article

Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele.

Journal of medical genetics - 1 Jul 2003

Perrault I, Hanein S, Gerber S, Barbet F, Dufier J-L, Munnich A, Rozet J-M, Kaplan J

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 12843339
DOI: 10.1136/jmg.40.7.e90
PMCID: PMC1735514

Genes

CRX

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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Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele.PMID 12843339Read ↗

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