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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 autism spectrum disorders, epilepsy and schizophrenia. Rece...

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Furkejuvvon:
Váldodahkkit: 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
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: BMC 2011-08-01
Ráidu:BMC Medical Genetics
Liŋkkat:http://www.biomedcentral.com/1471-2350/12/106
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