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Article

Genetic fine mapping of the gene for recessive Stargardt disease.

Human genetics - 1 Oct 1996

Hoyng C B, Poppelaars F, van de Pol T J, Kremer H, Pinckers A J, Deutman A F, Cremers F P

Abstract excerpt

Stargardt disease (STGD) is one of the most frequent causes of macular degeneration in childhood. Linkage analysis in families with recessive STGD has recently shown genetic homogeneity and a location of the underlying gene at 1p22-p21 in a 4-cM interval. Haplotype analysis in seven Dutch STGD families with 11 highly polymorphic markers spanning the critical region has enabled us to refine the location of the...

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PMID: 8792830
DOI: 10.1007/s004390050247

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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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