Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiency

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  2. Professor Rita Horvath
Author(s)Schrank B, Schoser B, Klopstock T, Schneiderat P, Horvath R, Abicht A, Holinski-Feder E, Augustis S
Publication type Article
JournalNeuromuscular Disorders
Year2017
Volume
IssueePub ahead of Print
Pages
ISSN (print)0960-8966
ISSN (electronic)1873-2364
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PublisherElsevier Ltd
URLhttp://doi.org/10.1016/j.nmd.2017.02.005
DOI10.1016/j.nmd.2017.02.005
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