KCNQ2 and KCNQ3 mutations in familial and sporadic cases of Benign Familial Neonatal Convulsions

Translated title of the contribution: KCNQ2 and KCNQ3 mutations in familial and sporadic cases of Benign Familial Neonatal Convulsions

N.E. Verbeek, M. Poot, F.E. Jansen, D. Lindhout, M.J.A. van Kempen

Research output: Contribution to conferencePosterOther research output

Translated title of the contributionKCNQ2 and KCNQ3 mutations in familial and sporadic cases of Benign Familial Neonatal Convulsions
Original languageUndefined/Unknown
Publication statusPublished - 2 Nov 2010
Event60th annual meeting of ASHG (American Society of Human Genetics) - Washington DC
Duration: 2 Nov 20106 Nov 2010

Conference

Conference60th annual meeting of ASHG (American Society of Human Genetics)
CityWashington DC
Period2/11/106/11/10

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde (GENK)
  • Geneeskunde(GENK)
  • Medical sciences
  • Bescherming en bevordering van de menselijke gezondheid

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