Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient

出版年份 2009 全文链接

标题

作者

关键词

出版物

Volume 19, Issue 2, Pages 143-146

出版商

Elsevier BV

发表日期

2009-01-22

DOI

10.1016/j.nmd.2008.11.016

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