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Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy
Weterman, M. A. J., Barth, P. G., van Spaendonck-Zwarts, K. Y., Aronica, E., Poll-The, B.-T., Brouwer, O. F., van Tintelen, J. P., Qahar, Z., Bradley, E. J., de Wissel, M., Salviati, L., Angelini, C.,Volume:
136
Language:
english
Journal:
Brain
DOI:
10.1093/brain/aws293
Date:
January, 2013
File:
PDF, 936 KB
english, 2013