학술논문
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Document Type
Article
Author
Koko, M.; Schubert, J.; Lerche, H.; Elseed, M.A.; Mohammed, I.N.; Hamed, A.A.; Abd Allah, A.S.I.; Siddig, R.A.; Elmahdi, E.O.; Elmugadam, F.A.; Eltaraifee, E.; Ali, N.M.H.; Malik, H.M.; Babai, A.M.; Yahia, A.; Altmüller, J.; Toliat, M.R.; Nürnberg, P.; Amin, M.; Ahmed, E.A.; Eltazi, I.Z.M.; Abdelgadir, W.A.; Ibrahim, M.O.M.; Bakhit, Y.H.; Ibrahim, M.E.; Salih, M.A.; Elsayed, L.E.O.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, 2024)
Subject
Language
English
ISSN
14765438
10184813
10184813