Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease-Reference-Cited by-同舟云学术

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Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

Published:1988-11 Issue:4 Volume:55 Page:601-610
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Wallace Douglas C.,Zheng Xianxian,Lott Marie T.,Shoffner John M.,Hodge Judith A.,Kelley Richard I.,Epstein Charles M.,Hopkins Linton C.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference42 articles.

1. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

2. Reduction in maximal oxygen uptake with age;Astrand;J. Appl. Physiol.,1973

3. A new method for detecting anaerobic threshold by gas exchange;Beaver;J. Appl. Physiol.,1986

4. Role of coenzyme Q in the mitochondrial respiratory chain;Brown;Biochemistry,1977

5. Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts;Case;Somatic Cell Genet,1981

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