CLCN1 Mutations in Czech Patients with Myotonia Congenita, In Silico Analysis of Novel and Known Mutations in the Human Dimeric Skeletal Muscle Chloride Channel

Lignende værker

• Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
  af: Stehlíková, Kristýna, et al.
  Udgivet: (2014)
• Myotonia congenita: novel mutations in CLCN1 gene
  af: Liu, Xiao-Li, et al.
  Udgivet: (2015)
• Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia
  af: Sun, Chen, et al.
  Udgivet: (2010)
• A Novel Mutation in CLCN1 Associated with Feline Myotonia Congenita
  af: Gandolfi, Barbara, et al.
  Udgivet: (2014)
• Novel CLCN1 Mutations and Clinical Features of Korean Patients with Myotonia Congenita
  af: Moon, In-Soo, et al.
  Udgivet: (2009)