Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints-Reference-Cited by-同舟云学术

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Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints

Published:2014-08-13 Issue:1 Volume:15 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

Dong Dawei W,Pereira Filipe,Barrett Steven P,Kolesar Jill E,Cao Kajia,Damas Joana,Yatsunyk Liliya A,Johnson F Brad,Kaufman Brett A

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

https://link.springer.com/content/pdf/10.1186/1471-2164-15-677.pdf

Reference67 articles.

1. Greaves LC, Reeve AK, Taylor RW, Turnbull DM: Mitochondrial DNA and disease. J Pathol. 2011, 226: 274-286.

2. Schon EA, DiMauro S, Hirano M: Human mitochondrial DNA: roles of inherited and somatic mutations. Nat Rev Genet. 2012, 13: 878-890.

3. Schaefer AM, McFarland R, Blakely EL, He L, Whittaker RG, Taylor RW, Chinnery PF, Turnbull DM: Prevalence of mitochondrial DNA disease in adults. Ann Neurol. 2008, 63: 35-39.

4. Schaefer AM, Taylor RW, Turnbull DM, Chinnery PF: The epidemiology of mitochondrial disorders–past, present and future. Biochim Biophys Acta. 2004, 1659: 115-120.

5. Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT, Taylor RW, Bindoff LA, Turnbull DM: The epidemiology of pathogenic mitochondrial DNA mutations. Ann Neurol. 2000, 48: 188-193.

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