Go to content
UR Home

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 and Grimm, T (1996) 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. British Journal of Ophthalmology 80 (8), pp. 745-749.

Full text not available from this repository.

at publisher (via DOI)

at PubMed


Abstract

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 ...

plus


Export bibliographical data



Item type:Article
Date:1996
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1136/bjo.80.8.745DOI
8949721PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:No
Item ID:35471
Owner only: item control page
  1. Homepage UR

University Library

Publication Server

Contact:

Publishing: oa@ur.de

Dissertations: dissertationen@ur.de

Research data: daten@ur.de

Contact persons