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

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

Detalhes bibliográficos
Principais autores: Hatton, C, Chen, J, Shelley, C, Croxen, R, Beeson, D, Colquhoun, D
Formato: Journal article
Publicado em: 2000
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Registros relacionados

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  • Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes (Retracted Article.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

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