Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children. (2014)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ymgme.2014.07.017
PubMed Identifier: 25087164
Publication URI: http://europepmc.org/abstract/MED/25087164
Type: Journal Article/Review
Volume: 113
Parent Publication: Molecular genetics and metabolism
Issue: 1-2
ISSN: 1096-7192