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


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Bibliographic Information

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PubMed Identifier: 25087164

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Type: Journal Article/Review

Volume: 113

Parent Publication: Molecular genetics and metabolism

Issue: 1-2

ISSN: 1096-7192