Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

Published 2011 View Full Article

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Title
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
Authors
Keywords
-
Journal
NEUROLOGY
Volume 77, Issue 6, Pages 540-548
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2011-07-14
DOI
10.1212/wnl.0b013e318228fc70

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