The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder.

Ítems similars

• The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder
  per: Muller, J, et al.
  Publicat: (2004)
• Chronic stridor as an early presentation of congenital myasthenic syndrome due to RAPSN mutation
  per: Mewasingh, L, et al.
  Publicat: (2006)
• Pathogenic mechanisms of RAPSN mutations in congenital myasthenic syndromes
  per: Cheung, JY
  Publicat: (2016)
• 126th International Workshop: congenital myasthenic syndromes, 24-26 September 2004, Naarden, the Netherlands.
  per: Beeson, D, et al.
  Publicat: (2005)
• A nomenclature and classification for the congenital myasthenic syndromes: preparing for FAIR data in the genomic era
  per: Thompson, R, et al.
  Publicat: (2018)