Recurrent KIF2A mutations are responsible for classic lissencephaly

Author(s):
Cavallin, M.; Bijlsma, E.K.; Morjani, A. el; Moutton, S.; Peeters, E.A.J.; Maillard, C.; Pedespan, J.M.; Guerrot, A.M.; Drouin-Garaud, V.; Coubes, C.; Genevieve, D.; Bole-Feysot, C.; Fourrage, C.; Steffann, J.; Bahi-Buisson, N.
Published
2017
Publication type
Article / Letter to editor
LissencephalyKinesinKIF2A
Date issued
2017-04-30
Language
English
Is part of
neurogenetics (2017), Vol. 18, no. 2, p. 73-79
hdl
1887/116299
doi
10.1007/s10048-016-0499-8