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Late Onset is Common in Best Macular Dystrophy Associated with VMD2 Gene Mutations

Renner, A B, Tillack, H, Kraus, H, Kramer, F, Mohr, N, Weber, Bernhard H. F. , Foerster, M H and Kellner, U (2005) Late Onset is Common in Best Macular Dystrophy Associated with VMD2 Gene Mutations. Ophthalmology 112 (4), pp. 586-592.

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Abstract

PURPOSE: To perform a detailed morphologic and functional evaluation of Best macular dystrophy (BMD) associated with mutations in the VMD2 gene. DESIGN: Retrospective study. PARTICIPANTS: The records of 16 patients with BMD and heterozygous VMD2 mutations (group 1) and 5 patients with Best-like lesions with no detectable disease-associated alterations in the VMD2 gene (group 2) were evaluated ...

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Item type:Article
Date:2005
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1016/j.ophtha.2004.10.041DOI
15808248PubMed 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:Partially
Item ID:35848
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