CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature

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dc.contributor.authorvan der Laan, Liselot
dc.contributor.authorSilva, Ananilia
dc.contributor.authorKleinendorst, Lotte
dc.contributor.authorRooney, Kathleen
dc.contributor.authorHaghshenas, Sadegheh
dc.contributor.authorLauffer, Peter
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorBhai, Pratibha
dc.contributor.authorBrusco, Alfredo
dc.contributor.authorde Munnik, Sonja
dc.contributor.authorde Vries, Bert B. A.
dc.contributor.authorVega, Angelica Delgado
dc.contributor.authorEngelen, Marc
dc.contributor.authorHerkert, Johanna C.
dc.contributor.authorHochstenbach, Ron
dc.contributor.authorHopman, Saskia
dc.contributor.authorKant, Sarina G.
dc.contributor.authorKira, Ryutaro
dc.contributor.authorKato, Mitsuhiro
dc.contributor.authorKeren, Boris
dc.contributor.authorKroes, Hester Y.
dc.contributor.authorLevy, Michael A.
dc.contributor.authorLock\\-Hock, Ngu
dc.contributor.authorMaas, Saskia M.
dc.contributor.authorMancini, Grazia M. S.
dc.contributor.authorMarcelis, Carlo
dc.contributor.authorMatsumoto, Naomichi
dc.contributor.authorMizuguchi, Takeshi
dc.contributor.authorMussa, Alessandro
dc.contributor.authorMignot, Cyril
dc.contributor.authorNarhi, Anu
dc.contributor.authorNordgren, Ann
dc.contributor.authorPfundt, Rolph
dc.contributor.authorPolstra, Abeltje M.
dc.contributor.authorTrajkova, Slavica
dc.contributor.authorvan Bever, Yolande
dc.contributor.authorvan den Boogaard, Marie Jose
dc.contributor.authorvan der Smagt, Jasper J.
dc.contributor.authorBarakat, Tahsin Stefan
dc.contributor.authorAlders, Marielle
dc.contributor.authorMannens, Marcel M. A. M.
dc.contributor.authorSadikovic, Bekim
dc.contributor.authorvan Haelst, Mieke M.
dc.contributor.authorHenneman, Peter
dc.date.accessioned2025-10-16T15:12:25Z
dc.date.issued2025
dc.identifier.doi10.1016/j.xhgg.2024.100380
dc.identifier.otherWOS:001364279900001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5427
dc.publisherELSEVIER
dc.sourceHUMAN GENETICS AND GENOMICS ADVANCES
dc.titleCUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature
dc.typeArticle

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