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Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.
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
The quasi-xgamma frailty model with survival analysis under heterogeneity problem, validation testing, and risk analysis for emergency care data.
Loubna H, Goual H, Alghamdi FM, Mustafa MS, Tekle Mekiso G, Ali MM, Al-Nefaie AH, Alsuhabi H, Ibrahim M, Yousof HM.
Loubna H, et al.
Sci Rep. 2024 Apr 18;14(1):8973. doi: 10.1038/s41598-024-59137-w.
Sci Rep. 2024.
PMID: 38637600
Free PMC article.
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Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report.
Amin M, Bakhit Y, Koko M, Ibrahim MOM, Salih MA, Ibrahim M, Seidi OA.
Amin M, et al. Among authors: ibrahim mom.
Acta Myol. 2019 Mar 1;38(1):21-24. eCollection 2019 Mar.
Acta Myol. 2019.
PMID: 31309178
Free PMC article.
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In Silico Analysis of SNPs in PARK2 and PINK1 Genes That Potentially Cause Autosomal Recessive Parkinson Disease.
Bakhit YH, Ibrahim MO, Amin M, Mirghani YA, Hassan MA.
Bakhit YH, et al.
Adv Bioinformatics. 2016;2016:9313746. doi: 10.1155/2016/9313746. Epub 2016 Dec 29.
Adv Bioinformatics. 2016.
PMID: 28127307
Free PMC article.
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