Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.

BACKGROUND: Autosomal recessive Stargardt's disease is a macular degeneration characterised by a juvenile onset and a rapidly progressive course resulting in an atrophic macular area typically surrounded by yellowish retinal flecks. METHOD: The disease locus has previously been assigned to mark...

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Detalhes bibliográficos
Main Authors: Weber, B H, Sander, S, Kopp, C, Walker, D, Eckstein, A, Wissinger, B, Zrenner, E, Grimm, T
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC505593/
https://ncbi.nlm.nih.gov/pubmed/8949721
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