Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.

Samankaltaisia teoksia

• The defect in a slow channel myasthenic syndrome mutant, epsilon L221F
  Tekijä: Hatton, C, et al.
  Julkaistu: (2000)
• Effects of epsilon L78P, an acetylcholine receptor mutation that causes slow channel congenital myasthenic syndrome.
  Tekijä: Shelley, C, et al.
  Julkaistu: (2003)
• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
  Tekijä: Croxen, R, et al.
  Julkaistu: (2002)
• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes (Retracted Article. See vol 72, pg 294, 2009)
  Tekijä: Croxen, R, et al.
  Julkaistu: (2002)
• Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
  Tekijä: Bonifati, D, et al.
  Julkaistu: (2004)