A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast-Reference-Cited by-同舟云学术

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

Published:2005-07 Issue:14 Volume:272 Page:3583-3592
ISSN:1742-464X
Container-title:FEBS Journal
language:en
Short-container-title:FEBS Journal

Author:

Blakely Emma L.,Mitchell Anna L.,Fisher Nicholas,Meunier Brigitte,Nijtmans Leo G.,Schaefer Andrew M.,Jackson Margaret J.,Turnbull Douglass M.,Taylor Robert W.

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1742-4658.2005.04779.x/fullpdf

Reference37 articles.

1. Sequence and organization of the human mitochondrial genome

2. Mitochondrial Respiratory-Chain Diseases

3. 4 RW Taylor, and DM Turnbull (2005 ) Mitochondrial DNA mutations in human disease . 6 , 389 -402 .

4. De novo mutations in the mitochondrialND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

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