An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect

标题
An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 91, Issue 4, Pages 737-743
出版商
Elsevier BV
发表日期
2012-09-27
DOI
10.1016/j.ajhg.2012.08.020

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