Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction

Neuromuscul Disord. 2012 May;22(5):478. doi: 10.1016/j.nmd.2012.02.001. Epub 2012 Mar 7.
No abstract available

Publication types

  • Letter
  • Comment
  • Published Erratum

MeSH terms

  • Family Health*
  • Female
  • Humans
  • Male
  • Mutation / genetics*
  • Myasthenic Syndromes, Congenital / genetics*
  • Myasthenic Syndromes, Congenital / physiopathology*
  • Phenotype*
  • Receptors, Nicotinic / genetics*
  • Siblings*

Substances

  • Receptors, Nicotinic