(Q60436411)
Statements
Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing (English)
Karen Gaudon
Isabelle Pénisson-Besnier
Brigitte Chabrol
Françoise Bouhour
Laurence Demay
Asma Ben Ammar
Christophe Vial
Guillaume Nicolas
Bruno Eymard