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A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect

Item Type:Article
Title:A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect
Creators Name:Thiselton, D.L. and Alexander, C. and Morris, A. and Brooks, S. and Rosenberg, T. and Eiberg, H. and Kjer, B. and Kjer, P. and Bhattacharya, S.S. and Votruba, M.
Source:Human Genetics
ISSN:0340-6717
Publisher:Springer (Germany)
Volume:109
Page Range:498-502
Date:1 November 2001
PubMed:View item in PubMed

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