Heterozygous truncating variants inSUFUcause congenital ocular motor apraxia

Schroeder, Simone; Li, Yun; Yigit, Gokhan; Altmueller, Janine; Bader, Ingrid; Bevot, Andrea; Biskup, Saskia; Dreha-Kulaczewski, Steffi; Korenke, G. Christoph; Kottke, Raimund; Mayr, Johannes A.; Preisel, Martin; Toelle, Sandra P.; Wente-Schulz, Sarah; Wortmann, Saskia B.; Hahn, Heidi; Boltshauser, Eugen; Uhmann, Anja; Wollnik, Bernd; Brockmann, Knut

dc.contributor.author	Bevot, Andrea
dc.date.accessioned	2021-05-18T07:59:25Z
dc.date.available	2021-05-18T07:59:25Z
dc.date.issued	2021
dc.identifier.issn	1530-0366
dc.identifier.uri	http://hdl.handle.net/10900/115270
dc.language.iso	en	de_DE
dc.publisher	Springernature	de_DE
dc.relation.uri	http://dx.doi.org/10.1038/s41436-020-00979-w	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Heterozygous truncating variants inSUFUcause congenital ocular motor apraxia	de_DE
dc.type	Article	de_DE
utue.quellen.id	20210304112512_01090
utue.publikation.seiten	341-351	de_DE
utue.personen.roh	Schroeder, Simone
utue.personen.roh	Li, Yun
utue.personen.roh	Yigit, Gokhan
utue.personen.roh	Altmueller, Janine
utue.personen.roh	Bader, Ingrid
utue.personen.roh	Bevot, Andrea
utue.personen.roh	Biskup, Saskia
utue.personen.roh	Dreha-Kulaczewski, Steffi
utue.personen.roh	Korenke, G. Christoph
utue.personen.roh	Kottke, Raimund
utue.personen.roh	Mayr, Johannes A.
utue.personen.roh	Preisel, Martin
utue.personen.roh	Toelle, Sandra P.
utue.personen.roh	Wente-Schulz, Sarah
utue.personen.roh	Wortmann, Saskia B.
utue.personen.roh	Hahn, Heidi
utue.personen.roh	Boltshauser, Eugen
utue.personen.roh	Uhmann, Anja
utue.personen.roh	Wollnik, Bernd
utue.personen.roh	Brockmann, Knut
dcterms.isPartOf.ZSTitelID	Genetics in Medicine	de_DE
dcterms.isPartOf.ZS-Issue	2	de_DE
dcterms.isPartOf.ZS-Volume	23	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE