OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

Published 2018 View Full Article

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Title
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
Authors
Keywords
-
Journal
EMBO Molecular Medicine
Volume -, Issue -, Pages e9060
Publisher
EMBO
Online
2018-09-10
DOI
10.15252/emmm.201809060

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