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...

詳細記述

書誌詳細

主要な著者:	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
フォーマット:	Artigo
言語:	Inglês
出版事項:	BMC 2011-08-01
シリーズ:	BMC Medical Genetics
オンライン･アクセス:	http://www.biomedcentral.com/1471-2350/12/106
タグ:	タグ追加 タグなし, このレコードへの初めてのタグを付けませんか!