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

Ижил төстэй зүйлс

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• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes (Retracted Article.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