Cousin, Margot A.,
Veale, Emma L.,
Dsouza, Nikita R.,
Tripathi, Swarnendu,
Holden, Robyn G.,
Arelin, Maria,
Beek, Geoffrey,
Bekheirnia, Mir Reza,
Beygo, Jasmin,
Bhambhani, Vikas,
and others.
Bialer, Martin,
Bigoni, Stefania,
Boelman, Cyrus,
Carmichael, Jenny,
Courtin, Thomas,
Cogne, Benjamin,
Dabaj, Ivana,
Doummar, Diane,
Fazilleau, Laura,
Ferlini, Alessandra,
Gavrilova, Ralitza H.,
Graham, John M.,
Haack, Tobias B.,
Juusola, Jane,
Kant, Sarina G.,
Kayani, Saima,
Keren, Boris,
Ketteler, Petra,
Klöckner, Chiara,
Koopmann, Tamara T.,
Kruisselbrink, Teresa M.,
Kuechler, Alma,
Lambert, Laëtitia,
Latypova, Xénia,
Lebel, Robert Roger,
Leduc, Magalie S.,
Leonardi, Emanuela,
Lewis, Andrea M.,
Liew, Wendy,
Machol, Keren,
Mardini, Samir,
McWalter, Kirsty,
Mignot, Cyril,
McLaughlin, Julie,
Murgia, Alessandra,
Narayanan, Vinodh,
Nava, Caroline,
Neuser, Sonja,
Nizon, Mathilde,
Ognibene, Davide,
Park, Joohyun,
Platzer, Konrad,
Poirsier, Céline,
Radtke, Maximilian,
Ramsey, Keri,
Runke, Cassandra K.,
Guillen Sacoto, Maria J.,
Scaglia, Fernando,
Shinawi, Marwan,
Spranger, Stephanie,
Tan, Ee Shien,
Taylor, John,
Trentesaux, Anne-Sophie,
Vairo, Filippo,
Willaert, Rebecca,
Zadeh, Neda,
Urrutia, Raul,
Babovic-Vuksanovic, Dusica,
Zimmermann, Michael T.,
Mathie, Alistair,
and
Klee, Eric W.
(hide)
(2022)
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome.
Genome Medicine,
14
(1).
Article Number 62.
E-ISSN 1756-994X.
(doi:10.1186/s13073-022-01064-4)
(KAR id:95466)
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