Disease‐related versus polymorphic mutations in human mitochondrial tRNAs-Reference-Cited by-同舟云学术

Disease‐related versus polymorphic mutations in human mitochondrial tRNAs

Published:2001-06 Issue:6 Volume:2 Page:481-486
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Florentz Catherine¹,Sissler Marie¹

Affiliation:

1. UPR 9002 du CNRS, Département Mécanismes et Macromolécules de la Synthèse Protéique et Cristallogenèse, Institut de Biologie Moléculaire et Cellulaire 15 rue René Descartes F‐67084 Strasbourg Cedex France

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1093/embo-reports/kve111

Reference25 articles.

1. Free-radical-induced mutation vs redox regulation: Costs and benefits of genes in organelles

2. Sequence and organization of the human mitochondrial genome

3. 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

4. Mitochondrial Encephalomyopathies

5. A tRNA suppressor mutation in human mitochondria

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