Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Published 2011 View Full Article

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Title
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 89, Issue 4, Pages 543-550
Publisher
Elsevier BV
Online
2011-10-13
DOI
10.1016/j.ajhg.2011.09.007

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