Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Author(s):
Gregor, A.; Albrecht, B.; Bader, I.; Bijlsma, E.K.; Ekici, A.B.; Engels, H.; Hackmann, K.; Horn, D.; Hoyer, J.; Klapecki, J.; Kohlhase, J.; Maystadt, I.; Nagl, S.; Prott, E.; Tinschert, S.; Ullmann, R.; Wohlleber, E.; Woods, G.; Reis, A.; Rauch, A.; Zweier, C.
Published
2011
Publication type
Article / Letter to editor
Date issued
2011-08-09
Language
English
Is part of
BMC Medical Genetics (2011), Vol. 12, p. -
hdl
1887/108794
doi
10.1186/1471-2350-12-106