APA

Yano S., Li L., Le T. P., Moseley K., Guedalia A., Lee J., Gonzalez I. & Boles R. G. (20040430). 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. : Journal of inherited metabolic disease.

Chicago

Yano S, Li L, Le T P, Moseley K, Guedalia A, Lee J, Gonzalez I and Boles R G. 20040430. 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. : Journal of inherited metabolic disease.

Harvard

Yano S., Li L., Le T. P., Moseley K., Guedalia A., Lee J., Gonzalez I. and Boles R. G. (20040430). 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. : Journal of inherited metabolic disease.

MLA

Yano S, Li L, Le T P, Moseley K, Guedalia A, Lee J, Gonzalez I and Boles R G. 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. : Journal of inherited metabolic disease. 20040430.