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Repurposing the inhibitors of COVID-19 key proteins through molecular docking approach.
Process Biochem. 2021 Nov;110:216-222. doi: 10.1016/j.procbio.2021.08.015. Epub 2021 Aug 17.
Process Biochem. 2021.
PMID: 34421325
Free PMC article.
Biallelic loss of function variant in ZNF808 is associated with non-syndromic neonatal diabetes.
Alqahtani MA, Al-Qahtani SM, Al-Falki YH, Alharby E, Albulym OM, Almontashiri NAM.
Alqahtani MA, et al. Among authors: albulym om.
Clin Genet. 2023 Oct;104(4):497-498. doi: 10.1111/cge.14389. Epub 2023 Jun 12.
Clin Genet. 2023.
PMID: 37308312
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Idiopathic Thrombocytosis in Alpha Thalassemia Trait Patient.
Makkawi M, Alasmari S, Albulym O, Alkhaldy H.
Makkawi M, et al. Among authors: albulym o.
Ann Clin Lab Sci. 2024 Jan;54(1):114-117.
Ann Clin Lab Sci. 2024.
PMID: 38514054
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MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.
Albulym OM, Kennerson ML, Harms MB, Drew AP, Siddell AH, Auer-Grumbach M, Pestronk A, Connolly A, Baloh RH, Zuchner S, Reddel SW, Nicholson GA.
Albulym OM, et al.
Ann Neurol. 2016 Mar;79(3):419-27. doi: 10.1002/ana.24575. Epub 2016 Jan 13.
Ann Neurol. 2016.
PMID: 26659848
Free PMC article.
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The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family.
Albulym OM, Zhu D, Reddel S, Kennerson M, Nicholson G.
Albulym OM, et al.
J Neurodegener Dis. 2013;2013:495873. doi: 10.1155/2013/495873. Epub 2012 Nov 28.
J Neurodegener Dis. 2013.
PMID: 26316991
Free PMC article.
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