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

Fritzen, Daniel; Kuechler, Alma; Grimmel, Mona; Becker, Jessica; Peters, Sophia; Sturm, Marc; Hundertmark, Hela; Schmidt, Axel; Kreiss, Martina; Strom, Tim M.; Wieczorek, Dagmar; Haack, Tobias B.; Beck-Woedl, Stefanie; Cremer, Kirsten; Engels, Hartmut

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	Article	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