Concepedia

Publication | Open Access

Mutations in potassium channel <i>kcnd3</i> cause spinocerebellar ataxia type 19

DOIFull Paper Access

134

Citations

35

References

2012

Year

Anna Duarri, Justyna Jezierska, Michiel R. Fokkens, Michel Meijer, Helenius J. Schelhaas, Wilfred F.A. den Dunnen, Freerk van Dijk, Corien C. Verschuuren‐Bemelmans, G. Hageman, Pieter van de Vlies,
Annals of Neurology

Abstract

KCND3 mutations cause SCA19 by impaired protein maturation and/or reduced channel function.

References

YearCitations

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