Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12

Goubau, Christophe; Devriendt, Koen; Van der Aa, Nathalie; Crepel, An; Wieczorek, Dagmar; Kleefstra, Tjitske; Willemsen, Marjolein H.; Rauch, Anita; Tzschach, Andreas; de Ravel, Thomy; Leemans, Peter; Van Geet, Chris; Buyse, Gunnar; Freson, Kathleen

dc.contributor.author	Tzschach, Andreas	de_DE
dc.date.accessioned	2014-02-03T14:22:34Z
dc.date.available	2014-02-03T14:22:34Z
dc.date.issued	2013	de_DE
dc.identifier.issn	1018-4813	de_DE
dc.identifier.uri	http://hdl.handle.net/10900/40418
dc.language.iso	en	en
dc.publisher	Nature Publishing Group	de_DE
dc.relation.uri	http://dx.doi.org/10.1038/ejhg.2013.86	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12	de_DE
dc.type	Article	de_DE
utue.quellen.id	20140116051827_00081	de_DE
utue.publikation.seiten	1349-1355	de_DE
utue.personen.roh	Goubau, Christophe	de_DE
utue.personen.roh	Devriendt, Koen	de_DE
utue.personen.roh	Van der Aa, Nathalie	de_DE
utue.personen.roh	Crepel, An	de_DE
utue.personen.roh	Wieczorek, Dagmar	de_DE
utue.personen.roh	Kleefstra, Tjitske	de_DE
utue.personen.roh	Willemsen, Marjolein H.	de_DE
utue.personen.roh	Rauch, Anita	de_DE
utue.personen.roh	Tzschach, Andreas	de_DE
utue.personen.roh	de Ravel, Thomy	de_DE
utue.personen.roh	Leemans, Peter	de_DE
utue.personen.roh	Van Geet, Chris	de_DE
utue.personen.roh	Buyse, Gunnar	de_DE
utue.personen.roh	Freson, Kathleen	de_DE
dcterms.isPartOf.ZSTitelID	European Journal of Human Genetics	de_DE
dcterms.isPartOf.ZS-Issue	12	de_DE
dcterms.isPartOf.ZS-Volume	21	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE