Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.
Luedde M; Ehlermann P; Weichenhan D; Will R; Zeller R; Rupp S; Müller A; Steen H; Ivandic BT; Ulmer HE; Kern M; Katus HA; Frey N; Cardiovascular Research, 2010, vol. 86, issue 3, p 452, ISSN 17553245. ISBN 17553245.

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