Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias

Published 2010 View Full Article

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Title
Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias
Authors
Keywords
-
Journal
HUMAN MUTATION
Volume 31, Issue 10, Pages 1117-1124
Publisher
Wiley
Online
2010-08-21
DOI
10.1002/humu.21342
References
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