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Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children. (2014)

First Author: Ivanov IS

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