Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy.
Weterman, Marian A. J.; Barth, Peter G.; van Spaendonck-Zwarts, Karin Y.; Aronica, Eleonora; Poll-The, Bwee-Tien; Brouwer, Oebele F.; van Tintelen, J. Peter; Qahar, Zohal; Bradley, Edward J.; de Wissel, Marit; Salviati, Leonardo; Angelini, Corrado; van den Heuvel, Lambertus; Thomasse, Yolande E. M.; Backx, Ad P.; Nürnberg, Gudrun; Nürnberg, Peter; Baas, Frank; Brain: A Journal of Neurology, 2013, vol. 136, issue 1, p 282, ISSN 00068950. ISBN 14602156.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef