De novo SPAST mutations may cause a complex SPG4 phenotype
- Author(s):
- Schieving, J.H.; Bot, S.T. de; Pol, L.A. van de; Wolf, N.I.; Brilstra, E.H.; Frints, S.G.; Gaalen, J. van; Misra-lsrie, M.; Pennings, M.; Verschuuren-Bemelmans, C.C.; Kamsteeg, E.J.; Warrenburg, B.P. van de; Willemsen, M.A.
- Published
- 2019
- Publication type
- Article / Letter to editor
- Date issued
- 2019-07-31
- Language
- English
- Is part of
- Brain
- hdl
- 1887/120629
- doi
- 10.1093/brain/awz140