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Article Dans Une Revue Neurology Année : 2008

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

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hal-03863833 , version 1 (21-11-2022)

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P. Richard, K. Gaudon, H. Haddad, A. Ammar, E. Genin, et al.. The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa. Neurology, 2008, 71 (24), pp.1967-1972. ⟨10.1212/01.wnl.0000336921.51639.0b⟩. ⟨hal-03863833⟩
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