Mitochondrial transporters of the SLC25 family and associated diseases: A review

Journal of Inherited Metabolic Disease

Volumn 37, Issue 4, 2014, Pages 565-575

  Palmieri, Ferdinando ^a  

^a UNIVERSITY OF BARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ACYLCARNITINE; ADENINE NUCLEOTIDE TRANSLOCASE; ASPARTIC ACID; CARNITINE; CITRIC ACID; GLUTAMIC ACID; PHOSPHATE TRANSPORTER; PROTEIN; SLC 25 PROTEIN; UNCLASSIFIED DRUG; ANION TRANSPORT PROTEIN; CARRIER PROTEIN;

AUTOSOMAL DOMINANT INHERITANCE; BRAIN DISEASE; CELL FUNCTION; CELL STRUCTURE; CELL TRANSPORT; CONFERENCE PAPER; ENERGY YIELD; ENZYME SPECIFICITY; EPILEPSY; HUMAN; HYPERORNITHINEMIA HYPERAMMONEMIA HOMOCITRULLINURIA SYNDROME; METABOLIC DISORDER; METABOLISM; MICROCEPHALY; MITOCHONDRIAL MEMBRANE; MITOCHONDRION; NEUROPATHY; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; PROTEIN FAMILY; RARE DISEASE; SIDEROBLASTIC ANEMIA; ANIMAL; CHEMICAL STRUCTURE; CHEMISTRY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETICS; INBORN ERROR OF METABOLISM; MULTIGENE FAMILY; PROTEIN CONFORMATION;

ANIMALS; ANION TRANSPORT PROTEINS; HUMANS; METABOLISM, INBORN ERRORS; MITOCHONDRIAL DISEASES; MITOCHONDRIAL MEMBRANE TRANSPORT PROTEINS; MODELS, MOLECULAR; MULTIGENE FAMILY; PROTEIN CONFORMATION;

EID: 84904125074     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-014-9708-5     Document Type: Article

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