Thiamine-Responsive Congenital Lactic Acidosis Without MC
DOI:
https://doi.org/10.15844/pedneurbriefs-19-8-3Keywords:
Congenital Lactic Acidosis, Mitochondrial Encephalomyopathy, CardiomyopathyAbstract
Six infants with thiamine-responsive congenital lactic acidosis (CLA), normal pyruvate dehydrogenase complex activity, and no evidence of mitochondrial encephalomyopathy, are reported from Tottori University, Yonago; National Children’s Medical Center, Tokyo, and other centers in Japan.Published
2005-08-01
Issue
Section
Mitochondrial Cytopathies
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