TY  - GEN
AU  - Yano,S
AU  - Li,L
AU  - Le,T P
AU  - Moseley,K
AU  - Guedalia,A
AU  - Lee,J
AU  - Gonzalez,I
AU  - Boles,R G
TI  - 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
SN  - 0141-8955
PY  - 2004///0430
KW  - Carbon-Carbon Ligases
KW  - deficiency
KW  - Child, Preschool
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Female
KW  - Gene Deletion
KW  - Humans
KW  - Infant
KW  - Male
KW  - Methylmalonic Acid
KW  - urine
KW  - Mitochondrial Diseases
KW  - Phenotype
KW  - Propionic Acidemia
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1023/a:1025125427868
ER  -