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P3.41. Clinical and genetic findings in a large cohort of patients with congenital myopathies due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene
A. Klein, S. Lillis, I. Oprea, M. Scoto, S. Robb, A. Manzur, V. Straub, H. Roper, P.Y. Jeannet, H. Kingston, U.B. Jensen, E. Wraige, N. Trump, W. Rakowicz, M. Roberts, C. Longman, H. Lochmuller, K. BuVolume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.935
File:
PDF, 49 KB
english, 2011