| 1 | KCND3, SCA19
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| Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.
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| Duarri A, Jezierska J, Fokkens M, Meijer M, Schelhaas HJ, den Dunnen WF, van Dijk F, Verschuuren-Bemelmans C, Hageman G, van de Vlies P, Küsters B, van de Warrenburg BP, Kremer B, Wijmenga C, Sinke RJ, Swertz MA, Kampinga HH, Boddeke E, Verbeek DS.
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| Ann Neurol 72(6):870-80. doi: 10.1002/ana.23700.
2012
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| 2 | KCND3, SCA19
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| Mutations in KCND3 cause spinocerebellar ataxia type 22.
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| Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW.
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| Ann Neurol 72(6):859-69. doi: 10.1002/ana.23701.
2012
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| 3 | KCND3, SCA19
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| Repolarization matters: mutations in the Kv4.3 potassium channel cause SCA19/22.
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| Pulst SM, Otis TS.
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| Ann Neurol 72(6):829-31. doi: 10.1002/ana.23803. No abstract available.
2012
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| 4 | SCA19
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| Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
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| Verbeek DS, Schelhaas JH, Ippel EF, Beemer FA, Pearson PL, Sinke RJ.
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| Hum Genet 111(4-5):388-93. 2002
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