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Best's Vitelliform Dystrophy (VMD2) Maps between D11S903 and PYGM: No Evidence for Locus Heterogeneity

Weber, Bernhard H. F. , Walker, D, Müller, B and Mar, L (1994) Best's Vitelliform Dystrophy (VMD2) Maps between D11S903 and PYGM: No Evidence for Locus Heterogeneity. Genomics 20 (2), pp. 267-274.

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Abstract

Vitelliform macular dystrophy, also known as Best's disease (BD), is an autosomal dominant disorder typically characterized by an accumulation of yellowish material in the macular area. The disease is slowly progressive and eventually results in atrophy of the retinal pigment epithelium and photoreceptor cells, thus severely impairing central vision. The biochemical defect underlying this ...

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Item type:Article
Date:1994
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1006/geno.1994.1163DOI
8020974PubMed 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:35359
Owner only: item control page
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