Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis

Gelijkaardige items

• Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
  door: Xu, Yang-Qi, et al.
  Gepubliceerd in: (2018)
• Myotonia congenita: novel mutations in CLCN1 gene
  door: Liu, Xiao-Li, et al.
  Gepubliceerd in: (2015)
• Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation
  door: Zhao, Chenyu, et al.
  Gepubliceerd in: (2020)
• Mutations of SCN4A gene cause different diseases: 2 case reports and literature review
  door: Liu, Xiao-li, et al.
  Gepubliceerd in: (2015)
• Myotonia congenita with strabismus in a large family with a mutation in the SCN4A gene
  door: Du, H, et al.
  Gepubliceerd in: (2012)