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