SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency

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Title
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency
Authors
Keywords
-
Journal
BRAIN
Volume 141, Issue 3, Pages 662-672
Publisher
Oxford University Press (OUP)
Online
2017-12-22
DOI
10.1093/brain/awx369

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