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.
Revue:
Neuromuscular Disorders

ISSN: 0960-8966 1873-2364

Année de publication: 2012

Volumen: 22

Número: 3

Pages: 231-243

Type: Article

DOI: 10.1016/J.NMD.2011.10.013 GOOGLE SCHOLAR

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