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Taylor R.W., Giordano C., Davidson M.M., d'Amati G., Bain H., Hayes C.M., Leonard H., Barron M.J., Casali C., Santorelli F.M., Hirano M., Lightowlers R.N., DiMauro S., Turnbull D.M. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy. - J.Am.Coll Cardiol., 2003, v. 41, p. 1786-1796.

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