Primary and secondary defects of the mitochondrial respiratory chain-Reference-Cited by-同舟云学术

Primary and secondary defects of the mitochondrial respiratory chain

Published:2002-05 Issue:3 Volume:25 Page:207-214
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Schapira A. H. V.¹

Affiliation:

1. ; University Department of Clinical Neurosciences, Royal Free and University College Medical School and Institute of Neurology; University College London; London NW3 2PF UK

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1015629912477/fullpdf

Reference11 articles.

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2. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency;Bourgeron;Nature Genetics,1995

3. A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene;Kadowaki;Muscle Nerve,1994

4. Role of adenine nucleotide translocator 1 in mtDNA maintenance;Kaukonen;Science,2000

5. Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia;Lodi;Proc Natl Acad Sci USA,1999

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