Literature DB >> 15965226

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

P Soltanzadeh, J S Müller, A Ghorbani, A Abicht, H Lochmüller, A Soltanzadeh.   

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Year:  2005        PMID： 15965226      PMCID： PMC1739705          DOI： 10.1136/jnnp.2004.059436

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  1 in total

1.  A retrospective review of 15 patients with familial myasthenia gravis over a period of 25 years.

Authors:  Hui-Yu Feng; Wei-Bin Liu; Chuan-Ming Luo; Li-Xuan Yang; Wei Fang; Li Qiu; Xin Huang; Yan Li; Ru-Xun Huang
Journal:  Neurol Sci       Date:  2011-11-05       Impact factor: 3.307
  1 in total

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