Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2

  1. Kamsteeg, E.-J.
  2. Kress, W.
  3. Catalli, C.
  4. Hertz, J.M.
  5. Witsch-Baumgartner, M.
  6. Buckley, M.F.
  7. Van Engelen, B.G.M.
  8. Schwartz, M.
  9. Scheffer, H.
Revue:
European Journal of Human Genetics

ISSN: 1018-4813 1476-5438

Année de publication: 2012

Volumen: 20

Número: 12

Pages: 1203-1208

Type: Article

DOI: 10.1038/EJHG.2012.108 GOOGLE SCHOLAR lock_openAccès ouvert editor

Objectifs de Développement Durable