Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency-Reference-Cited by-同舟云学术

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Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency

Published:1999-09 Issue:1 Volume:1455 Page:35-44
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

von Kleist-Retzow Jürgen-Christoph,Vial Elodie,Chantrel-Groussard Karine,Rötig Agnès,Munnich Arnold,Rustin Pierre,Taanman Jan-Willem

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference59 articles.

1. THE MITOCHONDRIAL ELECTRON TRANSPORT AND OXIDATIVE PHOSPHORYLATION SYSTEM

2. Biogenesis of Mitochondria

3. A High Rate (20%–30%) of Parental Consanguinity in Cytochrome-Oxidase Deficiency

4. The Whole Structure of the 13-Subunit Oxidized Cytochrome c Oxidase at 2.8 Å

5. The cytochrome oxidase superfamily of redox-driven proton pumps

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4. Mitochondrial Cytochrome c Oxidase Assembly in Health and Human Diseases;Mitochondrial Disorders Caused by Nuclear Genes;2012-09-18

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