Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy

Published 2010 View Full Article

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Title
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy
Authors
Keywords
-
Journal
Molecular Neurodegeneration
Volume 5, Issue 1, Pages 25
Publisher
Springer Nature
Online
2010-06-15
DOI
10.1186/1750-1326-5-25

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