ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy
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author: Thomas Meitinger, Thomas J Nicholls, Joanna Rorbach, Enrico Baruffini, Michał Mińczuk, Johannes A Mayr, Holger Prokisch, Robert William Taylor, Tobias B Haack, Katharina Danhauser, Thomas Wieland, Tim M Strom, Peter Freisinger, Robert Kopajtich, Ileana Ferrero, Ralf A. Husain, Jessica Schum
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