A-type voltage-gated potassium channel KCND3 isoform X2 [Homo sapiens]

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Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K(V)4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties. [Int J Mol Sci. 2021]
Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K(V)4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties.
Zanni G, Hsiao CT, Fu SJ, Tang CY, Capuano A, Bosco L, Graziola F, Bellacchio E, Servidei S, Primiano G, et al. Int J Mol Sci. 2021 May 7; 22(9). Epub 2021 May 7.
A Novel Gain-of-Function KCND3 Variant Associated with Brugada Syndrome. [Cardiology. 2020]
A Novel Gain-of-Function KCND3 Variant Associated with Brugada Syndrome.
Li X, Li Z, Wang DWW, Wang DW, Wang Y. Cardiology. 2020; 145(10):623-632. Epub 2020 Aug 20.
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern. [JCI Insight. 2019]
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern.
Teumer A, Trenkwalder T, Kessler T, Jamshidi Y, van den Berg ME, Kaess B, Nelson CP, Bastiaenen R, De Bortoli M, Rossini A, et al. JCI Insight. 2019 Dec 5; 4(23). Epub 2019 Dec 5.

RefSeq genomic sequence
See the genomic reference sequence for the KCND3 gene (NG_032011.2).
RefSeq mRNA
See reference mRNA sequence for the KCND3 gene (XM_011541425.4).
RefSeq protein isoforms
See 20 reference sequence protein isoforms for the KCND3 gene.

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