Mitochondrial DNA and RNA processing in MELAS
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference37 articles.
1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
2. Topical Review: Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes (MELAS): Current Concepts
3. Vascular involvement in mitochondrial myopathy
4. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
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1. Exploring the Ability of LARS2 Carboxy-Terminal Domain in Rescuing the MELAS Phenotype;Life;2021-07-10
2. Energetic costs of cellular and therapeutic control of stochastic mitochondrial DNA populations;PLOS Computational Biology;2019-06-26
3. Quantitative Variation in m.3243A > G Mutation Produce Discrete Changes in Energy Metabolism;Scientific Reports;2019-04-08
4. Clinical syndromes associated with mtDNA mutations: where we stand after 30 years;Essays in Biochemistry;2018-07-20
5. Energetic costs of cellular and therapeutic control of stochastic mtDNA populations;2017-06-02
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