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

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

<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...

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Main Authors: Ullmann Reinhard, Tinschert Sigrid, Prott Eva, Nagl Sandra, Maystadt Isabelle, Kohlhase Jürgen, Klapecki Jakub, Hoyer Juliane, Horn Denise, Hackmann Karl, Engels Hartmut, Ekici Arif B, Bijlsma Emilia K, Bader Ingrid, Albrecht Beate, Gregor Anne, Wohlleber Eva, Woods Geoffrey, Reis André, Rauch Anita, Zweier Christiane
Format: Article
Language:English
Published: BMC 2011-08-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/12/106

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