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1887
115080
Male patients affected by mosaic PCDH19 mutations: five new cases
Author(s):
Lange, I.M. de; Rump, P.; Neuteboom, R.F.; Augustijn, P.B.; Hodges, K.; Kistemaker, A.I.; Brouwer, O.F.; Mancini, G.M.S.; Newman, H.A.; Vos, Y.J.; Helbig, K.L.; Peeters-Scholte, C.; Kriek, M.; Knoers, N.V.; Lindhout, D.; Koeleman, B.P.C.; Kempen, M.J.A. van; Brilstra, E.H.
Published
2017
Publication type
Article / Letter to editor
PCDH19
Mosaicism
Epilepsy
Intellectual disability
Date issued
2017-07-31
Language
English
Is part of
neurogenetics (2017), Vol. 18, no. 3, p. 147-153
hdl
1887/115080
doi
10.1007/s10048-017-0517-5
Persistent identifier url
https://hdl.handle.net/1887/115080
Documents
01 - 10.1007-s10048-017-0517-5
version: Not Applicable (or Unknown)
Open Access