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Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.
Koko M, Elseed MA, Mohammed IN, Hamed AA, Abd Allah ASI, Yahia A, Siddig RA, Altmüller J, Toliat MR, Elmahdi EO, Amin M, Ahmed EA, Eltazi IZM, Elmugadam FA, Abdelgadir WA, Eltaraifee E, Ibrahim MOM, Ali NMH, Malik HM, Babai AM, Bakhit YH, Nürnberg P, Ibrahim ME, Salih MA, Schubert J, Elsayed LEO, Lerche H. Koko M, et al. Among authors: abdelgadir wa. Eur J Hum Genet. 2024 Feb 5. doi: 10.1038/s41431-024-01541-x. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38316952
A Satellite-Free Centromere in Equus przewalskii Chromosome 10.
Piras FM, Cappelletti E, Abdelgadir WA, Salamon G, Vignati S, Santagostino M, Sola L, Nergadze SG, Giulotto E. Piras FM, et al. Among authors: abdelgadir wa. Int J Mol Sci. 2023 Feb 18;24(4):4134. doi: 10.3390/ijms24044134. Int J Mol Sci. 2023. PMID: 36835543 Free PMC article.
Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy.
Dahawi M, Elmagzoub MS, A Ahmed E, Baldassari S, Achaz G, Elmugadam FA, Abdelgadir WA, Baulac S, Buratti J, Abdalla O, Gamil S, Alzubeir M, Abubaker R, Noé E, Elsayed L, Ahmed AE, Leguern E. Dahawi M, et al. Among authors: abdelgadir wa. Front Neurol. 2021 Oct 21;12:738272. doi: 10.3389/fneur.2021.738272. eCollection 2021. Front Neurol. 2021. PMID: 34744978 Free PMC article.