Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.


Møller R., Weber Y., Klitten L., Trucks H., Muhle H., Kunz W., ...More

Epilepsia, vol.54, pp.256-64, 2013 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 54
  • Publication Date: 2013
  • Doi Number: 10.1111/epi.12078
  • Journal Name: Epilepsia
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.256-64
  • Keywords: Idiopathic generalized epilepsy, 1q21, 1 microdeletion, Two-hit hypothesis, NRXN1, MODEL, MICRODELETIONS, PREDISPOSE, CHANNELS, SPECTRUM, GENOME, 1Q21.1, GENES, RISK
  • Bezmialem Vakıf University Affiliated: Yes