Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene.
Van Hove JL; Freehauf C; Miyamoto S; Vladutiu GD; Pancrudo J; Bonilla E; Lovell MA; Mierau GW; Thomas JA; Shanske S; European Journal Of Pediatrics, 2008, vol. 167, issue 7, p 771, ISSN 14321076. ISBN 14321076.

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