Mitochondrial complex I deficiency of nuclear origin I. Structural genes.

Pagniez-Mammeri, Hélène; Loublier, Sandrine; Legrand, Alain; Bénit, Paule; Rustin, Pierre; Slama, Abdelhamid

Pagniez-Mammeri, Hélène; Loublier, Sandrine; Legrand, Alain; Bénit, Paule; Rustin, Pierre; Slama, Abdelhamid.

Affiliation

Pagniez-Mammeri H; Laboratoire de Biochimie, APHP Hôpital de Bicêtre, 78 rue du Général Leclerc, 94275 Le Kremlin Bicêtre cedex, France.

Mol Genet Metab ; 105(2): 163-72, 2012 Feb.

Article in En | MEDLINE | ID: mdl-22142868

Subject(s)

Electron Transport Complex I/chemistry; Mitochondria/enzymology; Mitochondrial Diseases/enzymology; NADH Dehydrogenase/metabolism; Nuclear Proteins/metabolism; Electron Transport; Electron Transport Complex I/deficiency; Electron Transport Complex I/genetics; Genetic Association Studies; Humans; Mitochondrial Diseases/genetics; Mitochondrial Diseases/pathology; Mitochondrial Proteins/genetics; Mitochondrial Proteins/metabolism; Mutation; NADH Dehydrogenase/genetics; Nuclear Proteins/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nuclear Proteins / Mitochondrial Diseases / Electron Transport Complex I / Mitochondria / NADH Dehydrogenase Limits: Humans Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2012 Type: Article Affiliation country: France

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