Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency-Reference-Cited by-同舟云学术

Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency

Published:2015-02-26 Issue:11 Volume:24 Page:3238-3247
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Schiff Manuel,Haberberger Birgit,Xia Chuanwu,Mohsen Al-Walid,Goetzman Eric S.,Wang Yudong,Uppala Radha,Zhang Yuxun,Karunanidhi Anuradha,Prabhu Dolly,Alharbi Hana,Prochownik Edward V.,Haack Tobias,Häberle Johannes,Munnich Arnold,Rötig Agnes,Taylor Robert W.,Nicholls Robert D.,Kim Jung-Ja,Prokisch Holger,Vockley Jerry

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/24/11/3238/14143674/ddv074.pdf

Reference54 articles.

1. Acyl-CoA dehydrogenases: dynamic history of protein family evolution;Swigonova;J. Mol. Evol.,2009

2. A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency;He;Am. J. Hum. Genet.,2007

3. Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency;Haack;Nat. Genet.,2010

4. Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene;Gerards;Brain,2011

5. Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I;Nouws;Cell. Metab.,2010

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