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This is an update request for the document Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
by Anne Gregor, Beate Albrecht, Ingrid Bader, 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 Rauch and Christiane Zweier
Your paper was deposited in PubMed Central
and appears online at http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3162517
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