(Q71862329)
Statements
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiency (English)
A Munnich
J M Saudubray
J Taylor
C Charpentier
C Marsac
F Rocchiccioli
O Amedee-Manesme
F X Coude
J Frezal