Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
扩大与 CNTNAP2 和 NRXN1 缺陷相关的临床谱
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/1471-2350-12-106
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