Cardiolipin content in mitochondria from cultured skin fibroblasts harboring mutations in the mitochondrial ATP6 gene

Journal of Bioenergetics and Biomembranes

Volumn 43, Issue 6, 2011, Pages 683-690

  El Hafidi, Mohammed ^a   Meschini, Maria Chiara ^b   Rizza, Teresa ^b   Santorelli, Filippo M ^c   Bertini, Enrico ^b   Carrozzo, Rosalba ^b   Vázquez Memije, Martha Elisa ^d,e  

^a INSTITUTO NACIONAL DE CARDIOLOGÍA IGNACIO CHÁVEZ   (Mexico)

^b BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^c DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

^d INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

^e Cedimemm SC   (Mexico)

Author keywords

ATP6 mutations; Cardiolipin; Leigh syndrome; Mitochondria

Indexed keywords

CARDIOLIPIN; PHOSPHOLIPID;

ARTICLE; CODON; CONTROLLED STUDY; CULTURE MEDIUM; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MITOCHONDRIAL GENE; MITOCHONDRIAL MEMBRANE; MITOCHONDRION; SKIN FIBROBLAST;

AMINO ACID SUBSTITUTION; CARDIOLIPINS; CELLS, CULTURED; CHILD; CHILD, PRESCHOOL; FEMALE; FIBROBLASTS; HUMANS; LIPID PEROXIDATION; MALE; MITOCHONDRIA; MITOCHONDRIAL MEMBRANES; MITOCHONDRIAL PROTON-TRANSLOCATING ATPASES; MUTATION, MISSENSE; SKIN;

TETRA;

EID: 84857058605     PISSN: 0145479X     EISSN: 15736881     Source Type: Journal    
DOI: 10.1007/s10863-011-9387-y     Document Type: Article

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