De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies

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dc.contributor.author Grimmel, Mona
dc.contributor.author Sturm, Marc
dc.contributor.author Beck-Wödl, Stefanie
dc.contributor.author Haack, Tobias
dc.date.accessioned 2019-11-11T07:46:46Z
dc.date.available 2019-11-11T07:46:46Z
dc.date.issued 2018
dc.identifier.issn 1432-1203
dc.identifier.uri http://hdl.handle.net/10900/94532
dc.language.iso en de_DE
dc.publisher Springer de_DE
dc.relation.uri http://dx.doi.org/10.1007/s00439-018-1892-1 de_DE
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies de_DE
dc.type Artikel de_DE
utue.quellen.id 20190321153956_02715
utue.publikation.seiten 401-411 de_DE
utue.personen.roh Fritzen, Daniel
utue.personen.roh Kuechler, Alma
utue.personen.roh Grimmel, Mona
utue.personen.roh Becker, Jessica
utue.personen.roh Peters, Sophia
utue.personen.roh Sturm, Marc
utue.personen.roh Hundertmark, Hela
utue.personen.roh Schmidt, Axel
utue.personen.roh Kreiss, Martina
utue.personen.roh Strom, Tim M.
utue.personen.roh Wieczorek, Dagmar
utue.personen.roh Haack, Tobias B.
utue.personen.roh Beck-Woedl, Stefanie
utue.personen.roh Cremer, Kirsten
utue.personen.roh Engels, Hartmut
dcterms.isPartOf.ZSTitelID Human Genetics de_DE
dcterms.isPartOf.ZS-Issue 5 de_DE
dcterms.isPartOf.ZS-Volume 137 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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