Is mitochondrial tRNALeu(UUR)3291T>C mutation pathogenic?
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.3109/19401736.2012.674119
Reference14 articles.
1. MITOMAP: a human mitochondrial genome database--2004 update
2. A comparison of RNA folding measures
3. A New Point Mutation at Nucleotide Pair-3291 of the Mitochondrial Transfer-RNALeu(Uur) Gene in a Patient with Mitochondrial Myopathy, Encephalopathy, Lactic-Acidosis, and Stroke-Like Episodes (MELAS)
4. The Vienna RNA Websuite
5. Mitochondrial DNA mutations in disease and aging
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1. The mitochondrial tRNAThr G15930A may be a novel mutation associated with hearing impairment;Mitochondrial DNA Part B;2019-01-02
2. The expanding phenotype of MELAS caused by the m.3291T>C mutation in the MT-TL1 gene;Molecular Genetics and Metabolism Reports;2016-03
3. Mitochondrial tRNA mutations may be infrequent in hepatocellular carcinoma patients;Genetics and Molecular Research;2016
4. Mitochondrial transfer RNA variants and primary congenital glaucoma;Mitochondrial DNA Part A;2015-04-02
5. Transition of 1628C > T in mitochondrial tRNAValgene should not be regarded as a mutation associated with hypertrophic cardiomyopathy;Mitochondrial DNA;2014-08-06
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