Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene

  1. Mazón, M.J.
  2. Barros, F.
  3. De la Peña, P.
  4. Quesada, J.F.
  5. Escudero, A.
  6. Cobo, A.M.
  7. Pascual-Pascual, S.I.
  8. Gutiérrez-Rivas, E.
  9. Guillén, E.
  10. Arpa, J.
  11. Eraso, P.
  12. Portillo, F.
  13. Molano, J.
Journal:
Neuromuscular Disorders

ISSN: 0960-8966 1873-2364

Year of publication: 2012

Volume: 22

Issue: 3

Pages: 231-243

Type: Article

DOI: 10.1016/J.NMD.2011.10.013 GOOGLE SCHOLAR