Effects of epsilon L78P, an acetylcholine receptor mutation that causes slow channel congenital myasthenic syndrome.

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)
• The defect in a slow channel myasthenic syndrome mutant, epsilon L221F
  द्वारा: Hatton, C, और अन्य
  प्रकाशित: (2000)
• Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
  द्वारा: Croxen, R, और अन्य
  प्रकाशित: (2002)
• Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
  द्वारा: Bonifati, D, और अन्य
  प्रकाशित: (2004)
• A Missense Mutation in Epsilon-subunit of Acetylcholine Receptor Causing Autosomal Dominant Slow-channel Congenital Myasthenic Syndrome in a Chinese Family
  द्वारा: Jia-Ze Tan, और अन्य
  प्रकाशित: (2016-01-01)