Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

Ítems similars

• Recurrent and founder mutations in inherited cardiac diseases in the Netherlands
  per: van Tintelen, J.P., et al.
  Publicat: (2009)
• Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome
  per: Hofman, N., et al.
  Publicat: (2010)
• Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide
  per: Postema, P.G., et al.
  Publicat: (2009)
• Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
  per: van den Wijngaard, A., et al.
  Publicat: (2011)
• GENCOR: a national registry for patients and families suffering from a familial heart disease in the Netherlands
  per: Hermans, J.F., et al.
  Publicat: (2006)