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Summary Expression Phenotypes Gene Literature (3) GO Terms (13) Nucleotides (36) Proteins (25) Interactants (31) Wiki
XB-GENEPAGE-1014061

Papers associated with kcnh4



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Loss-of-function variant in KCNH3 is associated with global developmental delay, autistic behavior, insomnia, and nocturnal seizures., Bauer CK, Kortüm F, Möllring A, Grinstein L, Denecke J, Alawi M, Bähring R, Harms FL., Seizure. March 20, 2025; 129 14-21.   


TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization., Wallmeier J, Shiratori H, Dougherty GW, Edelbusch C, Hjeij R, Loges NT, Menchen T, Olbrich H, Pennekamp P, Raidt J, Werner C, Minegishi K, Shinohara K, Asai Y, Takaoka K, Lee C, Lee C, Griese M, Memari Y, Durbin R, Kolb-Kokocinski A, Sauer S, Wallingford JB, Hamada H, Omran H., Am J Hum Genet. August 4, 2016; 99 (2): 460-9.   


Distribution and functional properties of human KCNH8 (Elk1) potassium channels., Zou A, Lin Z, Humble M, Creech CD, Wagoner PK, Krafte D, Jegla TJ, Wickenden AD., Am J Physiol Cell Physiol. December 1, 2003; 285 (6): C1356-66.

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