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      A Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectoris

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      Neuromuscular Disorders
      Elsevier BV

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          Journal
          Neuromuscular Disorders
          Neuromuscular Disorders
          Elsevier BV
          09608966
          April 2012
          April 2012
          : 22
          : 4
          : 355-360
          Article
          10.1016/j.nmd.2011.10.024
          02e4ba01-649c-441a-870f-dd7414ace4e6
          © 2012

          https://www.elsevier.com/tdm/userlicense/1.0/

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