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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
Langue:
english
Pages:
13
DOI:
10.1007/s10633-007-9094-5
Date:
March, 2008
Fichier:
PDF, 537 KB
english, 2008