3697G>A in MT-ND1 is a causative mutation in mitochondrial disease

标题

作者

关键词

Leigh disease, Mitochondrial disease, Next Generation Sequencing, Heteroplasmy, Clinical genomics

出版物

Volume 28, Issue -, Pages 54-59

出版商

Elsevier BV

发表日期

2016-03-25

DOI

10.1016/j.mito.2016.03.006

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