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Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiency. (2017)

First Author: Schrank B

Attributed to: Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2017.02.005

PubMed Identifier: 28279569

Publication URI: http://europepmc.org/abstract/MED/28279569

Type: Journal Article/Review

Volume: 27

Parent Publication: Neuromuscular disorders : NMD

Issue: 5

ISSN: 0960-8966