Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00059-013-3950-8.pdf
Reference41 articles.
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2. Levinger L, Mörl M, Florentz C (2004) Mitochondrial tRNA 3’ end metabolism and human disease. Nucleic Acids Res 32:5430–5441
3. Taylor RW, Giordano C, Davidson MM et al (2003) Homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy. J Am Coll Cardiol 41:1786–1796
4. Maron BJ, Gardin JM, Flack JM et al (1995) Prevalence of hypertrophic cardiomyopathy in a general population of young adults: echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary artery risk development in (Young) adults. Circulation 92:785–789
5. Maron BJ, Moller JH, Seidman CE et al (1998) Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases: hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome. A statement for healthcare professionals from the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association. Circulation 98:1460–1471
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