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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

Weber, Bernhard H. F. ; Sander, S. ; Kopp, C. ; Walker, D. ; Eckstein, A. ; Wissinger, B. ; Zrenner, E. ; Grimm, T.



Zusammenfassung

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 markers from chromosome 1p21-p13 by genetic linkage analysis in eight multiplex Stargardt's disease ...

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