Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis-Reference-Cited by-同舟云学术

Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis

Published:2016-04-30 Issue:11 Volume:44 Page:5313-5329
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucleic Acids Res

Author:

Rygiel Karolina A.,Tuppen Helen A.,Grady John P.,Vincent Amy,Blakely Emma L.,Reeve Amy K.,Taylor Robert W.,Picard Martin,Miller James,Turnbull Doug M.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/44/11/5313/17436767/gkw382.pdf

Reference45 articles.

1. Mutations of mitochondrial DNA polymerase ?A are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

2. RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions

3. Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis

4. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

5. Mitochondrial DNA Rearrangements in Health and Disease-A Comprehensive Study

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