Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome

Chemistry and Physics of Lipids

Volumn 193, Issue , 2015, Pages 1-10

  Gaspard, Gerard J ^a   McMaster, Christopher R ^a  

^a DALHOUSIE UNIVERSITY   (Canada)

Author keywords

Barth syndrome; Cardiolipin; Cardiomyopathy; Electron transport chain; Glycerolipid; Inherited disease; Mitochondria; Mitophagy; Orphan disease; Phospholipid

Indexed keywords

ACYLTRANSFERASE; CARDIOLIPIN;

BARTH SYNDROME; CARDIOMYOPATHY; CYTOLOGY; FRUIT FLY MODEL; GENE; GENE MUTATION; HUMAN; INHERITED CARDIOMYOPATHY BARTH SYNDROME; LIPID METABOLISM; MAMMAL; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; QUALITY CONTROL; REVIEW; SACCHAROMYCES CEREVISIAE; TAZ GENE; YEAST; ANIMAL; METABOLISM; MITOCHONDRION; MITOPHAGY; PATHOLOGY;

ANIMALS; BARTH SYNDROME; CARDIOLIPINS; HUMANS; MITOCHONDRIA; MITOCHONDRIAL DEGRADATION;

EID: 84946207163     PISSN: 00093084     EISSN: 18732941     Source Type: Journal    
DOI: 10.1016/j.chemphyslip.2015.09.005     Document Type: Review

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