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

Lookup NU author(s): Dr Juliane Mueller, Professor Hanns Lochmuller

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Publication metadata

Author(s): Soltanzadeh P, Muller JS, Ghorbani A, Abicht A, Lochmuller H, Soltanzadeh A

Publication type: Letter

Publication status: Published

Journal: Journal of Neurology, Neurosurgery and Psychiatry

Year: 2005

Volume: 76

Issue: 7

Pages: 1039-1040

ISSN (print): 0022-3050

ISSN (electronic): 1468-330X

URL: http://dx.doi.org/10.1136/jnnp.2004.059436

DOI: 10.1136/jnnp.2004.059436

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