Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

BACKGROUND: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been associated with a wide spectrum of neuropsychiatric disorders such as developmental language and autism spectrum disorders, epilepsy and schizophrenia. Recently, homozygous or compound heterozygous d...

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Detalles Bibliográficos
Autores principales: Gregor, Anne, Albrecht, Beate, Bader, Ingrid, Bijlsma, Emilia K, Ekici, Arif B, Engels, Hartmut, Hackmann, Karl, Horn, Denise, Hoyer, Juliane, Klapecki, Jakub, Kohlhase, Jürgen, Maystadt, Isabelle, Nagl, Sandra, Prott, Eva, Tinschert, Sigrid, Ullmann, Reinhard, Wohlleber, Eva, Woods, Geoffrey, Reis, André, Rauch, Anita, Zweier, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162517/
https://www.ncbi.nlm.nih.gov/pubmed/21827697
http://dx.doi.org/10.1186/1471-2350-12-106

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162517/
https://www.ncbi.nlm.nih.gov/pubmed/21827697
http://dx.doi.org/10.1186/1471-2350-12-106

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