Mitochondria: A crossroads for lipid metabolism defect in neurodegeneration with brain iron accumulation diseases

International Journal of Biochemistry and Cell Biology

Volumn 63, Issue , 2015, Pages 25-31

  Aoun, Manar ^a   Tiranti, Valeria ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

CoA biosynthesis; Disease; Lipid metabolism; Mitochondria; Neurodegeneration

Indexed keywords

C19ORF12 PROTEIN, HUMAN; COASY PROTEIN, HUMAN; IRON; MITOCHONDRIAL PROTEIN; PANTOTHENATE KINASE; PHOSPHOLIPASE A2 GROUP VI; PHOSPHOLIPID; PHOSPHOTRANSFERASE; PLA2G6 PROTEIN, HUMAN; TRANSFERASE;

BRAIN; GENETICS; HUMAN; IRON METABOLISM DISORDER; LIPID METABOLISM; METABOLISM; MITOCHONDRION; MUTATION; PATHOLOGY;

BRAIN; GROUP VI PHOSPHOLIPASES A2; HUMANS; IRON; IRON METABOLISM DISORDERS; LIPID METABOLISM; MITOCHONDRIA; MITOCHONDRIAL PROTEINS; MUTATION; PHOSPHOLIPIDS; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); TRANSFERASES;

EID: 84930634952     PISSN: 13572725     EISSN: 18785875     Source Type: Journal    
DOI: 10.1016/j.biocel.2015.01.018     Document Type: Short Survey

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