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Publication
PropertyValue
Working Groups Winkelmann
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 34211179
DOIDOI 10.1038/s41588-021-00886-z
Publication Year2021
TitlePathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Wikidata
JournalNature genetics
ISSN1061-4036
ESSN1546-1718
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=34211179%5Buid%5D
Pages1006-1021
Issue7
Volume53
Journal AbbreviationNat Genet
AuthorsCousin MA, Creighton BA, Breau KA, Spillmann RC, Torti E, Dontu S, Tripathi S, Ajit D, Edwards RJ, Afriyie S, Bay JC, Harper KM, Beltran AA, Munoz LJ, Falcon Rodriguez L, Stankewich MC, Person RE, Si Y, Normand EA, Blevins A, May AS, Bier L, Aggarwal V, Mancini GMS, van Slegtenhorst MA, Cremer K, Becker J, Engels H, Aretz S, MacKenzie JJ, Brilstra E, van Gassen KLI, van Jaarsveld RH, Oegema R, Parsons GM, Mark P, Helbig I, McKeown SE, Stratton R, Cogne B, Isidor B, Cacheiro P, Smedley D, Firth HV, Bierhals T, Kloth K, Weiss D, Fairley C, Shieh JT, Kritzer A, Jayakar P, Kurtz-Nelson E, Bernier RA, Wang T, Eichler EE, van de Laar IMBH, McConkie-Rosell A, McDonald MT, Kemppainen J, Lanpher BC, Schultz-Rogers LE, Gunderson LB, Pichurin PN, Yoon G, Zech M, Jech R, Winkelmann J, Beltran AS, Zimmermann MT, Temple B, Moy SS, Klee EW, Tan QK, Lorenzo DN
First AuthorCousin MA
Last AuthorLorenzo DN
ScholiaScholia Wikidata-based representation at Scholia

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 Q112581863  Wikidata ID