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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. ; Kellner, U.



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 ...

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