Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
PRRT2双等位基因变异可能使人易患自限性家族性婴儿癫痫
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-024-01541-x
Koko, Mahmoud; Elseed, Maha A; Mohammed, Inaam N; Hamed, Ahlam A; Abd Allah, Amal S I; Yahia, Ashraf; Siddig, Rayan A; Altmüller, Janine; Toliat, Mohammad Reza; Elmahdi, Esra O; Amin, Mutaz; Ahmed, Elhami A; Eltazi, Isra Z M; Elmugadam, Fatima A; Abdelgadir, Wasma A; Eltaraifee, Esraa; Ibrahim, Mohamed O M; Ali, Nabila M H; Malik, Hiba M; Babai, Arwa M; Bakhit, Yousuf H; Nürnberg, Peter; Ibrahim, Muntaser E; Salih, Mustafa A; Schubert, Julian; Elsayed, Liena E O; Lerche, Holger