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ERG variability in X-linked congenital retinoschisis patients with mutations in theRS1gene and the diagnostic importance of fundus autofluorescence and OCT
Agnes B. Renner, Ulrich Kellner, Britta Fiebig, Elke Cropp, Michael H. Foerster, Bernhard H. F. WeberVolume:
116
Language:
english
Pages:
13
DOI:
10.1007/s10633-007-9094-5
Date:
March, 2008
File:
PDF, 537 KB
english, 2008