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.-Reference-Cited by-同舟云学术

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.

Published:1996-08-01 Issue:8 Volume:80 Page:745-749
ISSN:0007-1161
Container-title:British Journal of Ophthalmology
language:en
Short-container-title:British Journal of Ophthalmology

Author:

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

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference22 articles.

1. Uber familiare, progressive Degeneration in der Maculagegend des Auges;Stargardt, K.;Graefes Arch Ophthalmol

2. Stargardt's disease and fundus flavimaculatus;Noble, K.G.; Carr, R.E.;Arch Ophthalmol,1979

3. Clinical and genetic heterogeneity in retinitis pigmentosa;Kaplan, J.; Bonneau, D.; Frezal, J.; Munnich, A.; Dufier, J.L.;Hum Genet,1990

4. Dominantly inherited macular dystrophy with flecks (Stargardt);Cibis, G.W.; Morey, M.; Harris, D.J.;Arch Ophthalmol,1980

5. Dominant inheritance of Stargardt's disease;Bither, P.P.; Berns, L.A.;Am Optom Assoc,1988

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