Infantile mitochondrial DNA depletion syndrome associated with methylmalonic aciduria and 3-methylcrotonyl-CoA and propionyl-CoA carboxylase deficiencies in two unrelated patients: A new phenotype of mtDNA depletion syndrome

Author： Yano S.   Li L.   Le T.   Moseley K.   Guedalia A.   Lee J.   Gonzalez I.   Boles R.  

Publisher： Springer Publishing Company

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.26, Iss.5, 2003-07, pp. : 481-488

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