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

समान संसाधन

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