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

समान संसाधन

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• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes (Retracted Article.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