Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing - Vigipallia

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Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing

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Gaudon, K. | Penisson-Besnier, I. | Chabrol, B. | Bouhour, F. | Demay, L. | Ben Ammar, A. | Bauché, Stéphanie | Vial, C. | Nicolas, G. | Eymard, B. | Hantai, D. | Richard, P.

Edité par CCSD ; BMJ Publishing Group -

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Langue: en

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