Neuropathologic Aspects of Cytochrome C Oxidase Deficiency
Author:
Publisher
Wiley
Subject
Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.2000.tb00274.x/fullpdf
Reference73 articles.
1. Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome;Adams;Ann Neurol,1997
2. Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment;Amaravadi;Hum Genet,1997
3. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981
4. Exercise intolerance and mutations in the cytochrome b gene of mitochondrial DNA;Andreu;N Eng J Med,1999
5. Tissue-specific regulation of bovine heart cytochrome c oxidase activity by ADP via interaction with subunit VIa;Anthony;Proc Natl Acad Sci USA,1993
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