kcnd2 Literature

Gene Literature (42)

XB--952448

Papers associated with kcnd2 (and Disease Ontology)

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	KCND2 variants associated with global developmental delay differentially impair Kv4.2 channel gating., Zhang Y, Tachtsidis G, Schob C, Koko M, Hedrich UBS, Lerche H, Lemke JR, van Haeringen A, Ruivenkamp C, Prescott T, Tveten K, Gerstner T, Pruniski B, DiTroia S, VanNoy GE, Rehm HL, McLaughlin H, Bolz HJ, Zechner U, Bryant E, McDonough T, Kindler S, Bähring R., Hum Mol Genet. November 16, 2021; 30 (23): 2300-2314.
	Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1., Aidery P, Kisselbach J, Schweizer PA, Becker R, Katus HA, Thomas D., Gene. December 10, 2012; 511 (1): 26-33.

KCND2 variants associated with global developmental delay differentially impair Kv4.2 channel gating., Zhang Y, Tachtsidis G, Schob C, Koko M, Hedrich UBS, Lerche H, Lemke JR, van Haeringen A, Ruivenkamp C, Prescott T, Tveten K, Gerstner T, Pruniski B, DiTroia S, VanNoy GE, Rehm HL, McLaughlin H, Bolz HJ, Zechner U, Bryant E, McDonough T, Kindler S, Bähring R., Hum Mol Genet. November 16, 2021; 30 (23): 2300-2314.

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