Identification of FASTKD2 compound heterozygous mutations as the underlying cause of autosomal recessive MELAS-like syndrome

Published 2017 View Full Article

Authors

Keywords

MELAS, Mitochondrial encephalomyopathy, FASTKD2, Target sequencing, Korean

Journal

MITOCHONDRION

Volume 35, Issue -, Pages 54-58

Publisher

Elsevier BV

Online

2017-05-09

DOI

10.1016/j.mito.2017.05.005

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