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Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy

Title:	Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Authors:	Koko, Mahmoud^Aff1; Elseed, Maha A.^Aff2; Mohammed, Inaam N.^Aff2; Hamed, Ahlam A.^Aff2; Abd Allah, Amal S. I.^Aff3; Yahia, Ashraf^Aff4; Siddig, Rayan A.^Aff3; Altmüller, Janine^{Aff5, Aff6, Aff7}; Toliat, Mohammad Reza^Aff5; Elmahdi, Esra O.^Aff3; Amin, Mutaz^Aff8; Ahmed, Elhami A.^Aff9; Eltazi, Isra Z. M.^Aff10; Elmugadam, Fatima A.^Aff3; Abdelgadir, Wasma A.^Aff11; Eltaraifee, Esraa^Aff3; Ibrahim, Mohamed O. M.^Aff12; Ali, Nabila M. H.^Aff3; Malik, Hiba M.^Aff3; Babai, Arwa M.^Aff3; Bakhit, Yousuf H.^Aff13; Nürnberg, Peter^Aff5; Ibrahim, Muntaser E.^Aff14; Salih, Mustafa A.^{Aff15, Aff16}; Schubert, Julian^Aff1; Elsayed, Liena E. O.^{Aff17, IDs4143102401541x_cor26}; Lerche, Holger^Aff1
Source:	European Journal of Human Genetics. 32(10):1338-1342
Database:	Springer Nature Journals