ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy.
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Robert W. Taylor | M. Minczuk | T. Wieland | T. Meitinger | T. Strom | H. Prokisch | T. Haack | J. Rorbach | I. Ferrero | K. Danhauser | J. Mayr | R. Kopajtich | P. Freisinger | T. Nicholls | F. Zimmermann | H. Mundy | J. Schum | R. Husain | E. Baruffini | A. Walther | Robert W. Taylor