Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR) ]-Reference-Cited by-同舟云学术

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Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR) ]

Published:1991-07-29 Issue:1-2 Volume:286 Page:67-70
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Obermaier-Kusser B.,Paetzke-Brunner I.,Enter C.,Müller-Höcker J.,Zierz S.,Ruitenbeek W.,Gerbitz K.-D.

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(91)80942-V/fullpdf

Reference19 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. Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

4. Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

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1. Negative correlation between organ heteroplasmy, particularly hepatic heteroplasmy, and age at death revealed by post-mortem studies of m.3243A > G cases;Molecular Genetics and Metabolism;2023-11

2. Heteroplasmy and Copy Number in the Common m.3243A>G Mutation—A Post-Mortem Genotype–Phenotype Analysis;Genes;2020-02-18

3. Mitochondrial dysfunction, AMPK activation and peroxisomal metabolism: A coherent scenario for non-canonical 3-methylglutaconic acidurias;Biochimie;2020-01

4. Mitochondrial Medicine;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

5. Role of taurine in the pathologies of MELAS and MERRF;Amino Acids;2012-11-20

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