Mitochondrial DNA depletion and dGK gene mutations

Annals of Neurology

Volumn 52, Issue 3, 2002, Pages 311-317

  Salviati, Leonardo ^a,b   Sacconi, Sabrina ^a,c   Mancuso, Michelangelo ^a,d   Otaegui, David ^a   Camaño, Pilar ^a   Marina, Alberto ^a   Rabinowitz, Simon ^e   Shiffman, Rebecca ^f   Thompson, Karen ^g   Wilson, Claire M ^g   Feigenbaum, Annette ^h   Naini, Ali B ^a   Hirano, Michio ^a   Bonilla, Eduardo ^a   DiMauro, Salvatore ^a   Vu, Tuan H ^a,i  

^a College of Physicians and Surgeons ^*  (United States)

^b UNIVERSITY OF PADOVA   (Italy)

^c UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^d UNIVERSITY OF PISA   (Italy)

^e LONG ISLAND COLLEGE HOSPITAL   (United States)

^f NEW YORK METHODIST HOSPITAL   (United States)

^g KAPIOLANI MEDICAL CENTER FOR WOMEN AND CHILDREN   (United States)

^h HOSPITAL FOR SICK CHILDREN   (Canada)

ⁱ Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYGUANOSINE KINASE; MITOCHONDRIAL DNA;

ARTICLE; CLINICAL ARTICLE; FEMALE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INFANT; LIVER FAILURE; LIVER TRANSPLANTATION; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; SYNDROME;

AMINO ACID SEQUENCE; DNA, MITOCHONDRIAL; FEMALE; GENE DOSAGE; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INFANT; LIVER FAILURE; MALE; MUTATION, MISSENSE; PHENOTYPE; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PROTEIN STRUCTURE, TERTIARY;

EID: 0036714964     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10284     Document Type: Article

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