Transition of 1628C > T in mitochondrial tRNAValgene should not be regarded as a mutation associated with hypertrophic cardiomyopathy
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.3109/19401736.2014.945580
Reference17 articles.
1. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives
2. Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies
3. Is mitochondrial tRNASer(UCN)T7501C mutation associated with cardiovascular disease?
4. Is mitochondrial tRNALeu(UUR)3291T>C mutation pathogenic?
5. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases
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