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

Podobne zapisy

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