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Article

Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Jun 1999

Kerrison J B, Arnould V J, Ferraz Sallum J M, Vagefi M R, Barmada M M, Li Y, Zhu D, Maumenee I H

Abstract excerpt

OBJECTIVE: To evaluate a family with autosomal dominant optic atrophy, which has been previously linked to the Kidd blood group. DESIGN: Clinical evaluation with the assessment of visual acuity, color vision, and optic nerve appearance to determine affection status. Linkage analysis using polymorphic DNA markers. RESULTS: Visual acuities ranged from 20/20 to 6/200. Although linkage was excluded for chromosome...

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Identifiers

PMID: 10369594
DOI: 10.1001/archopht.117.6.805

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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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