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Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism.
Hum Genomics. 2024 Nov 21;18(1):130. doi: 10.1186/s40246-024-00659-9.
Hum Genomics. 2024.
PMID: 39574152
Free PMC article.
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: elmugadam fa.
Eur J Hum Genet. 2024 Oct;32(10):1338-1342. doi: 10.1038/s41431-024-01541-x. Epub 2024 Feb 5.
Eur J Hum Genet. 2024.
PMID: 38316952
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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: elmugadam fa.
Front Neurol. 2021 Oct 21;12:738272. doi: 10.3389/fneur.2021.738272. eCollection 2021.
Front Neurol. 2021.
PMID: 34744978
Free PMC article.
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