Cellular and functional analysis of four mutations located in the mitochondrial atpase6gene

Journal of Cellular Biochemistry

Volumn 106, Issue 5, 2009, Pages 878-886

  Vazquez Memije, Martha Elisa ^a   Rizza, Teresa ^b   Meschini, Maria Chiara ^b   Nesti, Claudia ^b   Santorelli, Filippo Maria ^b   Carrozzo, Rosalba ^b  

^a INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

^b BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

ATPase6 mutations; F1F0 ATPase; Leigh syndrome; Mitochondria; OS ATPase

Indexed keywords

ARGININE; PROTON; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ARTICLE; CYBRID; ENZYME ACTIVITY; GENE MUTATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; PHENOTYPE; PRIORITY JOURNAL;

ARGININE; CELLS, CULTURED; FIBROBLASTS; GENES, MITOCHONDRIAL; HUMANS; KINETICS; MITOCHONDRIAL PROTON-TRANSLOCATING ATPASES; MUTATION, MISSENSE; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; PROLINE;

EID: 65349190622     PISSN: 07302312     EISSN: 10974644     Source Type: Journal    
DOI: 10.1002/jcb.22055     Document Type: Article

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