Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation-Reference-Cited by-同舟云学术

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Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation

Published:2010-08 Issue:5 Volume:10 Page:497-509
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Kotarsky Heike,Karikoski Riitta,Mörgelin Matthias,Marjavaara Sanna,Bergman Petra,Zhang De-Liang,Smet Joél,van Coster Rudy,Fellman Vineta

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference68 articles.

1. The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1;Antonicka;Human Molecular Genetics,2006

2. Expression and developmental profile of antioxidant enzymes in human lung and liver;Asikainen;American Journal of Respiratory Cell and Molecular Biology,1998

3. Perl’s Prussian blue reaction for ferric iron;Bancroft,1996

4. Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ;Barel;American Journal of Human Genetics,2008

5. Mitochondrial oxygen sensing: regulation of hypoxia-inducible factor by mitochondrial generated reactive oxygen species;Bell;Essays in Biochemistry,2007

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