Blog
About

1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

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

      , , , , ,

      Neuromuscular Disorders

      Elsevier BV

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Related collections

          Author and article information

          Journal
          Neuromuscular Disorders
          Neuromuscular Disorders
          Elsevier BV
          09608966
          April 2012
          April 2012
          : 22
          : 4
          : 355-360
          Article
          10.1016/j.nmd.2011.10.024
          © 2012

          Comments

          Comment on this article