Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
- Gregor, Anne
- Albrecht, Beate
- Bader, Ingrid
- Bijlsma, Emilia K
- Ekici, Arif B
- Engels, Hartmut
- Hackmann, Karl
- Horn, Denise
- Hoyer, Juliane
- Klapecki, Jakub
- Kohlhase, Jürgen
- Maystadt, Isabelle
- Nagl, Sandra
- Prott, Eva
- Tinschert, Sigrid
- Ullmann, Reinhard
- Wohlleber, Eva
- Woods, Geoffrey
- Reis, André
- Rauch, Anita
- Zweier, Christiane
- 2011-8-9
Published in:
- BMC Medical Genetics. - Springer Science and Business Media LLC. - 2011, vol. 12, no. 1
- Language
-
- English
- Open access status
- gold
- Identifiers
-
- DOI 10.1186/1471-2350-12-106
- ISSN 1471-2350
- Persistent URL
- https://sonar.ch/global/documents/158105
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