Splice-site mutations in the achr epsilon subunit gene associated with congenital myasthenic syndrome

Benzer Materyaller

• Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
  Yazar:: Bonifati, D, ve diğerleri
  Baskı/Yayın Bilgisi: (2004)
• Myasthenia gravis in a woman with congenital AChR deficiency due to epsilon-subunit mutations.
  Yazar:: Croxen, R, ve diğerleri
  Baskı/Yayın Bilgisi: (2002)
• Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome.
  Yazar:: Webster, R, ve diğerleri
  Baskı/Yayın Bilgisi: (2004)
• Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes.
  Yazar:: Beeson, D, ve diğerleri
  Baskı/Yayın Bilgisi: (2003)
• End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.
  Yazar:: Croxen, R, ve diğerleri
  Baskı/Yayın Bilgisi: (2001)