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Query Trace: Seizures and CNNM2[original query]

The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2). Human mutation 2021 Feb . Franken Gijs A C, Müller Dominik, Mignot Cyril, Keren Boris, Lévy Jonathan, Tabet Anne-Claude, Germanaud David, Tejada Maria I, Kroes Hester Y, Nievelstein Rutger A J, Brimble Elise, Ruzhnikov Maria, Claverie-Martin Felix, Szczepanska Maria, Cuk Martin, Latta Femke, Konrad Martin, Martínez-Cruz Luis A, Bindels Bindels René J M, Hoenderop Joost G J, Schlingmann Karl-Peter, de Baaij Jeroen H Similar articles in PubMed
AS3MT Polymorphism: A Risk Factor for Epilepsy Susceptibility and Adverse Drug Reactions to Valproic Acid and Oxcarbazepine Treatment in Children From South China. Frontiers in neuroscience 2021 12 15 705297. Fan Xiaomei, Chen Yuna, Lu Jieluan, Li Wenzhou, Li Xi, Guo Huijuan, Chen Qing, Yang Yanxia, Xia Hanbi Similar articles in PubMed
Cyclin M2 (CNNM2) knockout mice show mild hypomagnesaemia and developmental defects. Scientific reports 2021 4 11 (1): 8217. Franken Gijs A C, Seker Murat, Bos Caro, Siemons Laura A H, van der Eerden Bram C J, Christ Annabel, Hoenderop Joost G J, Bindels René J M, Müller Dominik, Breiderhoff Tilman, de Baaij Jeroen H Similar articles in PubMed