The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines-Reference-Cited by-同舟云学术

The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines

Published:2002-02-13 Issue:3 Volume:19 Page:234-239
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bornstein Belén,Mas Jose Antonio,Fernández-Moreno Miguel Angel,Campos Yolanda,Martín Miguel Angel,del Hoyo Pilar,Rubio Juan Carlos,Arenas Joaquín,Garesse Rafael

Funder

DGICYT, Ministerio de Educación y Ciencia, Spain

Comunidad de Madrid

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference13 articles.

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2. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy;Arbustini;Am J Pathol,1998

3. A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers;Arenas;Neurology,1999

4. In vivo labeling and analysis of human mitochondrial translation products;Chomyn;Methods Enzymol,1996

5. Mutations in mtDNA: are we scraping the bottom of the barrel?;DiMauro;Brain Pathol,2000

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