Mutation analysis in 16 patients with mtDNA depletion.

Human mutation

Volumn 21, Issue 4, 2003, Pages 453-454

  Carrozzo, R ^a   Bornstein, B ^a   Lucioli, S ^a   Campos, Y ^a   de la Pena, P ^a   Petit, N ^a   Dionisi Vici, C ^a   Vilarinho, L ^a   Rizza, T ^a   Bertini, E ^a   Garesse, R ^a   Santorelli, F M ^a   Arenas, J ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYGUANOSINE KINASE; MITOCHONDRIAL DNA; PHOSPHOTRANSFERASE; THYMIDINE KINASE; THYMIDINE KINASE 2;

ARTICLE; CHILD; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYMOLOGY; EUROPE; FEMALE; GENETICS; HUMAN; INFANT; MALE; METABOLISM; METHODOLOGY; MORTALITY; MUSCLE MITOCHONDRION; MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; PATHOLOGY; PRESCHOOL CHILD; RETROSPECTIVE STUDY; SYNDROME;

AGE OF ONSET; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; EUROPE; FEMALE; HUMANS; INFANT; MALE; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL DISEASES; MUTATION; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); RETROSPECTIVE STUDIES; SYNDROME; THYMIDINE KINASE;

EID: 0037390960     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9135     Document Type: Article

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