CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
- Author(s):
- Groen, J.L.; Andrade, A.; Ritz, K.; Jalalzadeh, H.; Haagmans, M.; Bradley, T.E.J.; Jongejan, A.; Verbeek, D.S.; Nurnberg, P.; Denome, S.; Hennekam, R.C.M.; Lipscombe, D.; Baas, F.; Tijssen, M.A.J.
- Published
- 2015
- Publication type
- Article / Letter to editor
- Date issued
- 2015-02-15
- Language
- English
- Is part of
- Human Molecular Genetics (2015), Vol. 24, no. 4, p. 987-993
- hdl
- 1887/87944
- doi
- 10.1093/hmg/ddu513