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Low “penetrance” of phylogenetic knowledge in mitochondrial disease studies

  • Published:2005-07 Issue:1 Volume:333 Page:122-130
  • ISSN:0006-291X
  • Container-title:Biochemical and Biophysical Research Communications
  • language:en
  • Short-container-title:Biochemical and Biophysical Research Communications

Author:

Bandelt Hans-Jürgen,Achilli Alessandro,Kong Qing-Peng,Salas Antonio,Lutz-Bonengel Sabine,Sun Chang,Zhang Ya-Ping,Torroni Antonio,Yao Yong-Gang

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference43 articles.

1. Mitochondrial DNA recombination—no need to panic;Macaulay;Proc. R. Soc. London Ser. B,1999

2. The emerging limbs and twigs of the East Asian mtDNA tree;Kivisild;Mol. Biol. Evol.,2002

3. Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson’s disease;Ozawa;Biochem. Biophys. Res. Commun.,1991

4. Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson’s disease and mitochondrial encephalomyopathy;Ozawa;Biochem. Biophys. Res. Commun.,1991

5. Mechanism of somatic mitochondrial DNA mutations associated with age and diseases;Ozawa;Biochem. Biophys. Acta,1995

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