Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.

Anne Gregor, Beate Albrecht, Ingrid Bader (Co-author), Emilia K Bijlsma, Arif B Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki, Jürgen Kohlhase, Isabelle Maystadt, Sandra Nagl, Eva Prott, Sigrid Tinschert, Reinhard Ullmann, Eva Wohlleber, Geoffrey Woods, André Reis, Anita RauchChristiane Zweier

Research output: Contribution to journalOriginal Article (Journal)peer-review

97 Citations (Web of Science)
Original languageEnglish
Pages (from-to)106
JournalBMC MEDICAL GENETICS
Volume12
DOIs
Publication statusPublished - 2011

Keywords

  • LA-TOURETTE-SYNDROME
  • NEUREXIN SUPERFAMILY
  • STRUCTURAL VARIANTS
  • AUTISM
  • GENE
  • SCHIZOPHRENIA
  • DISRUPTION
  • DISORDERS
  • DELETIONS
  • GENOME

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