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Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula

Weber, Bernhard H. F. (1998) Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula. Acta anatomica 162 (2-3), pp. 65-74.

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Abstract

Hereditary dystrophies of the central retina and choroid are a heterogeneous group of disorders characterized by preferential loss of macular function and consequently loss of central and color vision. The primary causes leading to the degenerative processes are largely unknown although recent progress in human molecular genetics is most promising in providing novel insights into the basic ...

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Item type:Article
Date:1998
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1159/000046470DOI
9831752PubMed ID
Keywords:Macular dystrophy; ABCR transporter; Stargardt’s disease; Ataxin-7; SCA7; Guanylate cyclase-activating protein; Cone dystrophy; Cone-rod homeobox-containing gene; Tissue inhibitor of metalloproteinases-3; Sorsby fundus dystrophy; X-linked juvenile retinoschisis; Macular degeneration, age-related
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:35504
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