Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome

Published 2015 View Full Article

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Title
Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome
Authors
Keywords
Leigh syndrome, Mitochondria, NDUFV2, Complex I, Exome sequencing
Journal
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Volume 19, Issue 5, Pages 525-532
Publisher
Elsevier BV
Online
2015-05-14
DOI
10.1016/j.ejpn.2015.05.002

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