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

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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., Alexander, C., Morris, A., Brooks, S., Rosenberg, T., Eiberg, H., Kjer, B., Kjer, P., Bhattacharya, S.S. and Votruba, M.
Source:	Human Genetics
ISSN:	0340-6717
Publisher:	Springer
Volume:	109
Page Range:	498-502
Date:	1 November 2001
PubMed:	View item in PubMed

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