The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder.
Main Authors: | Müller, J, Abicht, A, Burke, G, Cossins, J, Richard, P, Baumeister, S, Stucka, R, Eymard, B, Hantaï, D, Beeson, D, Lochmüller, H |
---|---|
格式: | Journal article |
语言: | English |
出版: |
2004
|
相似书籍
-
The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder
由: Muller, J, et al.
出版: (2004) -
Chronic stridor as an early presentation of congenital myasthenic syndrome due to RAPSN mutation
由: Mewasingh, L, et al.
出版: (2006) -
Pathogenic mechanisms of RAPSN mutations in congenital myasthenic syndromes
由: Cheung, JY
出版: (2016) -
126th International Workshop: congenital myasthenic syndromes, 24-26 September 2004, Naarden, the Netherlands.
由: Beeson, D, et al.
出版: (2005) -
A nomenclature and classification for the congenital myasthenic syndromes: preparing for FAIR data in the genomic era
由: Thompson, R, et al.
出版: (2018)