Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.
Dimmock, D P
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. [electronic resource] - Human mutation Feb 2008 - 330-1 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
1098-1004
10.1002/humu.9519 doi
Adolescent
Child, Preschool
DNA, Mitochondrial--genetics
Female
Humans
Infant
Infant, Newborn
Male
Mutation--genetics
Organ Specificity
Phosphotransferases (Alcohol Group Acceptor)--genetics
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. [electronic resource] - Human mutation Feb 2008 - 330-1 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
1098-1004
10.1002/humu.9519 doi
Adolescent
Child, Preschool
DNA, Mitochondrial--genetics
Female
Humans
Infant
Infant, Newborn
Male
Mutation--genetics
Organ Specificity
Phosphotransferases (Alcohol Group Acceptor)--genetics