Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome.
Genome Medicine
Cousin, Margot A MA; Veale, Emma L EL; Dsouza, Nikita R NR; Tripathi, Swarnendu S; Holden, Robyn G RG; Arelin, Maria M; Beek, Geoffrey G; Bekheirnia, Mir Reza MR; Beygo, Jasmin J; Bhambhani, Vikas V; Bialer, Martin M; Bigoni, Stefania S; Boelman, Cyrus C; Carmichael, Jenny J; Courtin, Thomas T; Cogne, Benjamin B; Dabaj, Ivana I; Doummar, Diane D; Fazilleau, Laura L; Ferlini, Alessandra A; Gavrilova, Ralitza H RH; Graham, John M JM; Haack, Tobias B TB; Juusola, Jane J; Kant, Sarina G SG; Kayani, Saima S; Keren, Boris B; Ketteler, Petra P; Klöckner, Chiara C; Koopmann, Tamara T TT; Kruisselbrink, Teresa M TM; Kuechler, Alma A; Lambert, Laëtitia L; Latypova, Xénia X; Lebel, Robert Roger RR; Leduc, Magalie S MS; Leonardi, Emanuela E; Lewis, Andrea M AM; Liew, Wendy W; Machol, Keren K; Mardini, Samir S; McWalter, Kirsty K; Mignot, Cyril C; McLaughlin, Julie J; Murgia, Alessandra A; Narayanan, Vinodh V; Nava, Caroline C; Neuser, Sonja S; Nizon, Mathilde M; Ognibene, Davide D; Park, Joohyun J; Platzer, Konrad K; Poirsier, Céline C; Radtke, Maximilian M; Ramsey, Keri K; Runke, Cassandra K CK; Guillen Sacoto, Maria J MJ; Scaglia, Fernando F; Shinawi, Marwan M; Spranger, Stephanie S; Tan, Ee Shien ES; Taylor, John J; Trentesaux, Anne-Sophie AS; Vairo, Filippo F; Willaert, Rebecca R; Zadeh, Neda N; Urrutia, Raul R; Babovic-Vuksanovic, Dusica D; Zimmermann, Michael T MT; Mathie, Alistair A; Klee, Eric W EW