Persistent URL of this record https://hdl.handle.net/1887/120629
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De novo SPAST mutations may cause a complex SPG4 phenotype
- All authors
- 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.
- Date
- 2019-07-31
- Journal
- Brain
- Volume
- 142