Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency-Reference-Cited by-同舟云学术

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Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

Published:2003-08-12 Issue:20 Volume:12 Page:2693-2702
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Antonicka H.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/12/20/2693/6948197/ddg284.pdf

Cited by 221 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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