Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy.
Weterman MA; Barth PG; van Spaendonck-Zwarts KY; Aronica E; Poll-The BT; Brouwer OF; van Tintelen JP; Qahar Z; Bradley EJ; de Wissel M; Salviati L; Angelini C; van den Heuvel L; Thomasse YE; Backx AP; Nürnberg G; Nürnberg P; Baas F; Brain: A Journal Of Neurology, 2013, vol. 136, issue Pt 1, p 282, ISSN 14602156. ISBN 14602156.

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