Expanding the clinical spectrum associated with defects in <it>CNTNAP2 </it>and <it>NRXN1</it>

• Autors principals: Ullmann Reinhard (Autor), Tinschert Sigrid (Autor), Prott Eva (Autor), Nagl Sandra (Autor), Maystadt Isabelle (Autor), Kohlhase Jürgen (Autor), Klapecki Jakub (Autor), Hoyer Juliane (Autor), Horn Denise (Autor), Hackmann Karl (Autor), Engels Hartmut (Autor), Ekici Arif B (Autor), Bijlsma Emilia K (Autor), Bader Ingrid (Autor), Albrecht Beate (Autor), Gregor Anne (Autor), Wohlleber Eva (Autor), Woods Geoffrey (Autor), Reis André (Autor), Rauch Anita (Autor), Zweier Christiane (Autor)
• Format: Llibre
• Publicat: BMC, 2011-08-01T00:00:00Z.
• Matèries: article
• Accés en línia: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Heterozygous copy-number and missense variants in <it>CNTNAP2 </it>and <it>NRXN1 </it>have repeatedly been associated with a wide spectrum of neuropsychiatric disorders such as developmental language and autis...