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Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.
Nat Commun. 2020 Jan 30;11(1):595. doi: 10.1038/s41467-020-14360-7.
Nat Commun. 2020.
PMID: 32001716
Free PMC article.
Benign Pericardial Schwannoma: Case Report and Summary of Previously Reported Cases.
Almobarak AA, AlShammari A, Alhomoudi RI, Eshaq AM, Algain SM, Jensen EC, Mohammed S, Al-Kattan K, Kayali Z, AlAmodi AA.
Almobarak AA, et al. Among authors: algain sm.
Am J Case Rep. 2018 Jan 24;19:90-94. doi: 10.12659/ajcr.907408.
Am J Case Rep. 2018.
PMID: 29362352
Free PMC article.
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