Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases-Reference-Cited by-同舟云学术

Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases

Published:2005-04-29 Issue:13 Volume:579 Page:2948-2952
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Yasukawa Takehiro,Kirino Yohei,Ishii Norie,Holt Ian J.,Jacobs Howard T.,Makifuchi Takao,Fukuhara Nobuyoshi,Ohta Shigeo,Suzuki Tsutomu,Watanabe Kimitsuna

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Reference35 articles.

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

2. A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)

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

4. Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation

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