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Author Kably B |
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Belaidi H ; Regragui W ; Kably B ; Urtizberea JA ; Ouazzani R | 2008Myotonia congenita (MC) can be Autosomal recessive (Becker) or Autosomal dominant (Thomsen). These 2 forms are due to mutations in CLCN1 gene coding for chloride channel of muscle membrane. This is a study of the clinical and electrophysiologica[...]Article
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