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Browsing by Author Verbeek, D.S.

Full Text	Issue Date	Title	Author(s)
	2012	Mutations in KCND3 gene cause spinocerebellar ataxia type 19	Duarri, A.; Jezierska, J.; Fokkens, M.; Meijer, M.; Schelhaas, H.J., et al
	2012	Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19	Duarri, A.; Jezierska, J.; Fokkens, M.; Meijer, M.; Schelhaas, H.J., et al
	2011	Genetics of the dominant ataxias.	Verbeek, D.S.; Warrenburg, B.P.C. van de
	2005	Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.	Verbeek, D.S.; Warrenburg, B.P.C. van de; Hennekam, F.A.; Dooijes, D.; Ippel, P.F., et al
	2004	Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.	Verbeek, D.S.; Warrenburg, B.P.C. van de; Wesseling, P.; Pearson, P.L.; Kremer, H.P.H., et al
	2004	SCA19 and SCA22: evidence for one locus with a worldwide distribution.	Schelhaas, H.J.; Verbeek, D.S.; Warrenburg, B.P.C. van de; Sinke, R.J.