Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion-Reference-Cited by-同舟云学术

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Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion

Published:2003-10-22 Issue:11 Volume:11 Page:896-898
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Crimi Marco,Bo Roberto Del,Galbiati Sara,Sciacco Monica,Bordoni Andreina,Bresolin Nereo,Comi Giacomo Pietro

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201056.pdf

Reference8 articles.

1. Wallace DC, Brown MD, Lott MT : Mitochondrial DNA variation in human evolution and disease. Gene 1999; 238: 211–230, Review.

2. Zeviani M, Moraes CT, DiMauro S et al: Deletions of mitochondrial DNA in Kearns-Sayre syndrome. Neurology 1998; 51: 1525–1532.

3. Macaulay V, Richards M, Hickey E et al: The emerging tree of west Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs. Am J Hum Genet 1999; 64: 232–249.

4. Sternberg D, Danan C, Lombes A et al: Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders. Hum Mol Genet 1998; 7: 33–42.

5. Pulkes T, Sweeney MG, Hanna MG : Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. Lancet 2000; 356: 2068–2069.

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