Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing (Q60436411)
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scientific article published on 07 October 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing |
scientific article published on 07 October 2010 |
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