Novel CLCN1 mutation in a young male with Becker Myotonia and unique clinical phenotype

  • F Hoche, M Theis, M Qirshi, M Laufs, N Schmitz, S Vlaho, M Kieslich
  • Neuropediatrics, April 2012, Thieme Publishing Group
  • DOI: 10.1055/s-0032-1307193

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The following have contributed to this page: Professor Matthias Kieslich