Arnold GL; Salazar D; Neidich JA; Suwannarat P; Graham BH; Lichter-Konecki U; Bosch AM; Cusmano-Ozog K; Enns G; Wright EL; Lanpher BC; Owen NN; Lipson MH; Cerone R; Levy P; Wong L-J C; Dezsőfi A
(2012)
Introduction: 3-Methyl CoA carboxylase (3-MCC) deficiency is an inborn error of metabolism in the catabolism of the amino acid leucine. Original reports suggested this disorder was associated with significant neurological ...