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G.P.11.10 Partial genomic deletions of RAPSN account for 15% of congenital myasthenic syndrome after negative DNA sequencing
P. Richard, K. Gaudon, I. Pénisson-Besnier, B. Chabrol, F. Bouhour, C. Vial, A. Ben Ammar, S. Bauché, B. Eymard, D. HantaiVolume:
19
Year:
2009
Language:
english
DOI:
10.1016/j.nmd.2009.06.257
File:
PDF, 42 KB
english, 2009