Publications
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Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D et al..
2019.
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.. Acta Neuropathol.
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AlShail E, Alahmari ANasser, Dababo AAM, Alsagob M, Al-Hindi H, Khalil H, Masseri ZAl, AlSalamah R, Almohseny E, Alduhaish A et al..
2023.
A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome.. Front Oncol. 13:1034292.