PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Published:2013-05-12 Issue:17 Volume:22 Page:3477-3484
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Eschbach J.,Schwalenstocker B.,Soyal S. M.,Bayer H.,Wiesner D.,Akimoto C.,Nilsson A.-C.,Birve A.,Meyer T.,Dupuis L.,Danzer K. M.,Andersen P. M.,Witting A.,Ludolph A. C.,Patsch W.,Weydt P.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/22/17/3477/17259707/ddt202.pdf

Reference42 articles.

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4. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

5. PGC-1 coactivators: inducible regulators of energy metabolism in health and disease

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