Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

Author(s):
Bena, F.; Bruno, D.L.; Eriksson, M.; Ravenswaaij-Arts, C. van; Stark, Z.; Dijkhuizen, T.; Gerkes, E.; Gimelli, S.; Ganesamoorthy, D.; Thuresson, A.C.; Labalme, A.; Till, M.; Bilan, F.; Pasquier, L.; Kitzis, A.; Dubourgm, C.; Rossi, M.; Bottani, A.; Gagnebin, M.; Sanlaville, D.; Gilbert-Dussardier, B.; Guipponi, M.; Haeringen, A. van; Kriek, M.; Ruivenkamp, C.; Antonarakis, S.E.; Anderlid, B.M.; Slater, H.R.; Schoumans, J.
Published
2013
Publication type
Article / Letter to editor
NRXN1neurexinexondeletionautismseizuresreview
Date issued
2013-06-30
Language
English
Is part of
hdl
1887/102688
doi
10.1002/ajmg.b.32148