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Publication
PropertyValue
Working Groups Winkelmann
SubprojectNone
Open AccessNo
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 39301775
DOIDOI 10.1002/ana.27077
Publication Year2024
TitleLoss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.
JournalAnnals of neurology
ISSN0364-5134
ESSN1531-8249
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=39301775%5Buid%5D
Journal AbbreviationAnn Neurol
AuthorsBlackburn PR, Ebstein F, Hsieh TC, Motta M, Radio FC, Herkert JC, Rinne T, Thiffault I, Rapp M, Alders M, Maas S, Gerard B, Smol T, Vincent-Delorme C, Cogné B, Isidor B, Vincent M, Bachmann-Gagescu R, Rauch A, Joset P, Ferrero GB, Ciolfi A, Husson T, Guerrot AM, Bacino C, Macmurdo C, Thompson SS, Rosenfeld JA, Faivre L, Mau-Them FT, Deb W, Vignard V, Agrawal PB, Madden JA, Goldenberg A, Lecoquierre F, Zech M, Prokisch H, Necpál J, Jech R, Winkelmann J, Koprušáková MT, Konstantopoulou V, Younce JR, Shinawi M, Mighton C, Fung C, Morel CF, Lerner-Ellis J, DiTroia S, Barth M, Bonneau D, Krapels I, Stegmann APA, van der Schoot V, Brunet T, Bußmann C, Mignot C, Zampino G, Wortmann SB, Mayr JA, Feichtinger RG, Courtin T, Ravelli C, Keren B, Ziegler A, Hasadsri L, Pichurin PN, Klee EW, Grand K, Sanchez-Lara PA, Krüger E, Bézieau S, Klinkhammer H, Krawitz PM, Eichler EE, Tartaglia M, Küry S, Wang T
First AuthorBlackburn PR
Last AuthorWang T