Persistent URL of this record https://hdl.handle.net/1887/87944
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CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
- All authors
- 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.
- Date
- 2015-02-15
- Journal
- Human Molecular Genetics
- Volume
- 24
- Issue
- 4
- Pages
- 987 - 993