Genetic and clinical heterogeneity of RYR1-related myopathies in a cohort of 60 Dutch families with identification of 40 novel mutations

Author(s):
Voermans, N.C.; Jungbluth, H.; Raaphorst, J.; Snoeck, M.; Straathof, C.; Schelhaas, H.J.; Sie, L.; Coo, R. de; Pol, W. van de; Visser, M. de; Scheffer, H.; Kamsteeg, E.J.; Engelen, B.G.M. van
Published
2012
Publication type
Article / Letter to editor
Date issued
2012-10-31
Language
English
Is part of
Neuromuscular Disorders (2012), Vol. 22, no. 9-10, p. 841-841
hdl
1887/99555
doi
10.1016/j.nmd.2012.06.131