Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene-Reference-Cited by-同舟云学术

Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

Published:2010-10-07 Issue:1 Volume:134 Page:210-219
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Gerards Mike,van den Bosch Bianca J. C.,Danhauser Katharina,Serre Valérie,van Weeghel Michel,Wanders Ronald J. A.,Nicolaes Gerry A. F.,Sluiter Wim,Schoonderwoerd Kees,Scholte Hans R.,Prokisch Holger,Rötig Agnès,de Coo Irenaeus F. M.,Smeets Hubert J. M.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/134/1/210/16695939/awq273.pdf

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5. Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome;Benit;J Med Genet,2004

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