De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
ATP1A3基因的新生突变会导致儿童交替性偏瘫。
期刊:Nature Genetics
影响因子:29
doi:10.1038/ng.2358
Heinzen, Erin L; Swoboda, Kathryn J; Hitomi, Yuki; Gurrieri, Fiorella; Nicole, Sophie; de Vries, Boukje; Tiziano, F Danilo; Fontaine, Bertrand; Walley, Nicole M; Heavin, Sinéad; Panagiotakaki, Eleni; Fiori, Stefania; Abiusi, Emanuela; Di Pietro, Lorena; Sweney, Matthew T; Newcomb, Tara M; Viollet, Louis; Huff, Chad; Jorde, Lynn B; Reyna, Sandra P; Murphy, Kelley J; Shianna, Kevin V; Gumbs, Curtis E; Little, Latasha; Silver, Kenneth; Ptáček, Louis J; Haan, Joost; Ferrari, Michel D; Bye, Ann M; Herkes, Geoffrey K; Whitelaw, Charlotte M; Webb, David; Lynch, Bryan J; Uldall, Peter; King, Mary D; Scheffer, Ingrid E; Neri, Giovanni; Arzimanoglou, Alexis; van den Maagdenberg, Arn M J M; Sisodiya, Sanjay M; Mikati, Mohamad A; Goldstein, David B