Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy-Reference-Cited by-同舟云学术

Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy

Published:2014-09-06 Issue:1 Volume:16 Page:1-9
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Ajroud-Driss Senda,Fecto Faisal,Ajroud Kaouther,Lalani Irfan,Calvo Sarah E.,Mootha Vamsi K.,Deng Han-Xiang,Siddique Nailah,Tahmoush Albert J.,Heiman-Patterson Terry D.,Siddique Teepu

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-014-0421-1.pdf

Reference25 articles.

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