학술논문

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Document Type
article
Author
Holger HengelCélia Bosso-LefèvreGeorge GradyEmmanuelle Szenker-RaviHankun LiSarah PierceÉlise LebigotThong-Teck TanMichelle Y. EioGunaseelan NarayananKagistia Hana UtamiMonica YauNader HandalWerner DeigendeschReinhard KeimerHiyam M. MarzouqaMeral Gunay-AygunMichael J. MurielloHelene VerhelstSarah WeckhuysenSonal MahidaSakkubai NaiduTerrence G. ThomasJiin Ying LimEe Shien TanDamien HayeMichèl A. A. P. WillemsenRenske OegemaWendy G. MitchellTyler Mark PiersonMarisa V. AndrewsMarcia C. WillingLance H. RodanTahsin Stefan BarakatMarjon van SlegtenhorstRalitza H. GavrilovaDiego MartinelliTal GilboaAbdullah M. TamimMais O. HashemMoeenaldeen D. AlSayedMaha M. AbdulrahimMohammed Al-OwainAli AwajiAdel A. H. MahmoudEissa A. FaqeihAli Al AsmariSulwan M. AlgainLamyaa A. JadHesham M. AldhalaanIngo HelbigDavid A. KoolenAngelika RiessIngeborg Kraegeloh-MannPeter BauerSuleyman GulsunerHannah StambergerAlvin Yu Jin NgSha TangSumanty TohariBoris KerenLaura E. Schultz-RogersEric W. KleeSabina BarresiMarco TartagliaHagar Mor-ShakedSateesh MaddirevulaAmber BegtrupAida TelegrafiRolph PfundtRebecca SchüleBrian CirunaCarine BonnardMahmoud A. PouladiJames C. StewartAdam Claridge-ChangDirk J. LefeberFowzan S. AlkurayaAjay S. MathuruByrappa VenkateshJoseph J. BaryckiMelanie A. SimpsonSaumya S. JamuarLudger SchölsBruno Reversade
Source
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Subject
Science
Language
English
ISSN
2041-1723
Abstract
UDP-glucuronic acid is a component of the extracellular matrix. Here, the authors report biallelic variants in the gene encoding UDP-Glucose 6-Dehydrogenase (UGDH) in individuals affected by developmental epileptic encephalopathies that impair UGDH stability, oligomerization, or enzymatic activity in vitro.