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

标题
Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome
作者
关键词
Leigh syndrome, Mitochondria, NDUFV2, Complex I, Exome sequencing
出版物
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Volume 19, Issue 5, Pages 525-532
出版商
Elsevier BV
发表日期
2015-05-14
DOI
10.1016/j.ejpn.2015.05.002

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