reviewNew England Journal of MedicineJun 25, 2003Closed access

Mitochondrial Respiratory-Chain Diseases

Columbia University

PubMed
Indexed incrossrefpubmed

Abstract

The mitochondrial respiratory chain has the crucial function of supplying the cell with energy in the form of ATP. Mutations affecting this chain can arise in mitochondrial or nuclear DNA and cause diseases known as mitochondrial encephalomyopathies. Because the rules of inheritance of mitochondrial and nuclear DNA differ considerably, these brain–muscle syndromes often have unpredictable clinical and genetic features.

Citation impact

1,642
total citations
FWCI
28.63
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100%
References
87
Citations per year

Authors

2

Topics & keywords

Keywords
  • Mitochondrial Encephalomyopathies
  • Mitochondrial DNA
  • Mitochondrial respiratory chain
  • Respiratory chain
  • Human mitochondrial genetics
  • Nuclear DNA
  • Mitochondrial myopathy
  • Medicine
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