The defect in a slow channel myasthenic syndrome mutant, epsilon L221F

مواد مشابهة

• Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.
  حسب: Hatton, C, وآخرون
  منشور في: (2003)
• Effects of epsilon L78P, an acetylcholine receptor mutation that causes slow channel congenital myasthenic syndrome.
  حسب: Shelley, C, وآخرون
  منشور في: (2003)
• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
  حسب: Croxen, R, وآخرون
  منشور في: (2002)
• Recessive inheritance and variable pentrance of slow channel myasthenic syndromes
  حسب: Besson, D, وآخرون
  منشور في: (2002)
• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes (Retracted Article. See vol 72, pg 294, 2009)
  حسب: Croxen, R, وآخرون
  منشور في: (2002)