Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations.

Samankaltaisia teoksia

• Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations
  Tekijä: Cossins, J, et al.
  Julkaistu: (2006)
• AChR deficiency due to epsilon-subunit mutations: two common mutations in the Netherlands.
  Tekijä: Faber, C, et al.
  Julkaistu: (2009)
• A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition.
  Tekijä: Cossins, J, et al.
  Julkaistu: (2004)
• Myasthenia gravis in a woman with congenital AChR deficiency due to epsilon-subunit mutations.
  Tekijä: Croxen, R, et al.
  Julkaistu: (2002)
• Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
  Tekijä: Bonifati, D, et al.
  Julkaistu: (2004)