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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, Karl 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 ...