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  5. Myasthenia- familial

Myasthenia- familial

December 31, 2014

Latest Research

  • A Case of Congenital Myasthenia Gravis due to ChAT Gene Mutation in a Term Neonate: A Case Report
  • A family with early onset myopathy caused by MEGF10 gene defect and literature review
  • A novel <em>DOK7</em> mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members
  • A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members
  • A Rare Case of Lambert-Eaton Myasthenia Syndrome Associated with Non-Hodgkin's Lymphoma: A Case Report and Review of the Literature
More Research
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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