Male patients affected by mosaic PCDH19 mutations: five new cases

Lange, I.M. de; Rump, P.; Neuteboom, R.F.; Augustijn, P.B.; Hodges, K.; Kistemaker, A.I.; ... ; Brilstra, E.H. (2017)

Article / Letter to editor

• PCDH19
• Mosaicism
• Epilepsy
• Intellectual disability

• All authors: 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.
• Date: 2017-07-31
• Journal: neurogenetics
• Volume: 18
• Issue: 3
• Pages: 147 - 153
• DOI: doi:10.1007/s10048-017-0517-5