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C.P.3 Genetic and clinical heterogeneity of RYR1-related myopathies in a cohort of 60 Dutch families with identification of 40 novel mutations
Voermans, N.C., Jungbluth, H., Raaphorst, J., Snoeck, M., Straathof, C., Schelhaas, H.J., Sie, L., de Coo, R., van de Pol, W., de Visser, M., Scheffer, H., Kamsteeg, E.J., van Engelen, B.G.M.Volume:
22
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2012.06.131
Date:
October, 2012
File:
PDF, 46 KB
english, 2012