The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes-Reference-Cited by-同舟云学术

The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes

Published:2000-06 Issue:25 Volume:275 Page:19198-19209
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Chomyn Anne,Enriquez José Antonio,Micol Vicente,Fernandez-Silva Patricio,Attardi Giuseppe

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference59 articles.

1. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation

2. A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness

3. Mitochondrial mutation associated with nonsyndromic deafness

4. MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination

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