Browsing by Author "Hoyer, Juliane"

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Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Gregor, Anne; Albrecht, Beate; Bader, Ingrid; Bijlsma, Emilia K.; Ekici, Arif B.; Engels, Hartmut; Hackmann, KarlHorn, DeniseHoyer, JulianeKlapecki, JakubKohlhase, JurgenMaystadt, IsabelleNagl, SandraPrott, EvaTinschert, SigridUllmann, ReinhardWohlleber, EvaWoods, GeoffreyReis, AndreRauch, AnitaZweier, Christiane et al. (2011-08-09)

Abstract 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 ...