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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Номзүйн дэлгэрэнгүй

Үндсэн зохиолчид:	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
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	BMC 2011-08-01
Цуврал:	BMC Medical Genetics
Онлайн хандалт:	http://www.biomedcentral.com/1471-2350/12/106
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!