Pathogenic mutations of the human mitochondrial citrate carrier SLC25A1 lead to impaired citrate export required for lipid, dolichol, ubiquinone and sterol synthesis

Author:

Majd Homa,King Martin S.,Smith Anthony C.,Kunji Edmund R.S.

Funder

Medical Research Council

Cambridge Trust

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry,Biophysics

Reference47 articles.

1. Citrate and the conversion of carbohydrate into fat. Fatty acid synthesis by a combination of cytoplasm and mitochondria;Watson;J. Biol. Chem.,1970

2. Organization and sequence of the human gene for the mitochondrial citrate transport protein;Iacobazzi;DNA Seq.,1997

3. Kinetic study of tricarboxylate carrier in rat-liver mitochondria;Palmieri;Eur. J. Biochem.,1972

4. Factors affecting the kinetics and equilibrium of exchange reactions of the citrate-transporting system of rat liver mitochondria;Robinson;J. Biol. Chem.,1971

5. Tricarboxylate carrier of bovine liver mitochondria. Purification and reconstitution;Claeys;J. Biol. Chem.,1989

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