An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X) | Journal of Neurology, Neurosurgery & Psychiatry

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An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X)

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Cite this article as:: Soltanzadeh P, Müller JS, Ghorbani A, et al

An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X)

Journal of Neurology, Neurosurgery & Psychiatry 2005;76:1039-1040.