Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria-Reference-Cited by-同舟云学术

Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria

Published:2011-06-30 Issue:18 Volume:39 Page:8173-8186
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucleic Acids Research

Author:

Karicheva O. Z.,Kolesnikova O. A.,Schirtz T.,Vysokikh M. Y.,Mager-Heckel A.-M.,Lombes A.,Boucheham A.,Krasheninnikov I. A.,Martin R. P.,Entelis N.,Tarassov I.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/39/18/8173/3819902/gkr546.pdf

Reference56 articles.

1. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

2. The epidemiology of pathogenic mitochondrial DNA mutations

3. Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

4. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children

5. An enhanced MITOMAP with a global mtDNA mutational phylogeny

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