OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance

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Item Type:	Article
Title:	OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
Creators Name:	Pesch, U.E., Leo-Kottler, B., Mayer, S., Jurklies, B., Kellner, U., Apfelstedt-Sylla, E., Zrenner, E., Alexander, C. and Wissinger, B.
Source:	Human Molecular Genetics
ISSN:	0964-6906
Publisher:	Oxford University Press
Volume:	10
Page Range:	1359-1368
Date:	15 June 2001
PubMed:	View item in PubMed

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