Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency-Reference-Cited by-同舟云学术

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Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

Published:2000-03-22 Issue:5 Volume:9 Page:795-801
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/9/5/795/9815159/090795.pdf

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