Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts-Reference-Cited by-同舟云学术

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Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Published:2001-12-01 Issue:26 Volume:10 Page:3025-3035
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Jaksch M.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/10/26/3025/9813609/103025.pdf

Cited by 112 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Identification of a novel homozygous synthesis of cytochrome c oxidase 2 variant in siblings with early‐onset axonal Charcot‐Marie‐Tooth disease;Human Mutation;2022-02-16

3. An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases;Biomolecules;2021-11-04

4. Loss of Functional SCO2 Attenuates Oxidative Stress in Diabetic Kidney Disease;Diabetes;2021-10-26

5. The molecular and cellular basis of copper dysregulation and its relationship with human pathologies;The FASEB Journal;2021-08-14

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