Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes-Reference-Cited by-同舟云学术

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Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

Published:2010-12-20 Issue:12 Volume:5 Page:e15687
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Sadikovic Bekim,Wang Jing,El-Hattab Ayman,Landsverk Megan,Douglas Ganka,Brundage Ellen K.,Craigen William J.,Schmitt Eric S.,Wong Lee-Jun C.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference31 articles.

1. Mitochondrial DNA mutations in disease, aging, and neurodegeneration.;AK Reeve;Ann N Y Acad Sci,2008

2. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.;IJ Holt;Nature,1988

3. Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.;IJ Holt;Nucleic Acids Res,1989

4. Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988.;M Zeviani;Neurology,1998

5. Mitochondrial DNA and disease.;SR Hammans;Essays Biochem,1994

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