Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus

Mayer, Anja K.; Mahajnah, Muhammad; Thomas, Mervyn G.; Cohen, Yuval; Habib, Adib; Schulze, Martin; Maconachie, Gail D. E.; AlMoallem, Basamat; De Baere, Elfride; Lorenz, Birgit; Traboulsi, Elias, I; Kohl, Susanne; Azem, Abdussalam; Bauer, Peter; Gottlob, Irene; Sharkia, Rajech; Wissinger, Bernd

dc.contributor.author	Schulze, Martin
dc.contributor.author	Kohl, Susanne
dc.contributor.author	Bauer, Peter
dc.contributor.author	Wissinger, Bernd
dc.contributor.author	Mayer, Anja Kathrin
dc.date.accessioned	2020-03-19T16:23:21Z
dc.date.available	2020-03-19T16:23:21Z
dc.date.issued	2019
dc.identifier.issn	1460-2156
dc.identifier.uri	http://hdl.handle.net/10900/99200
dc.language.iso	en	de_DE
dc.publisher	Oxford Univ Press	de_DE
dc.relation.uri	http://dx.doi.org/10.1093/brain/awz098	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190926111821_01024
utue.publikation.seiten	1528-1534	de_DE
utue.personen.roh	Mayer, Anja K.
utue.personen.roh	Mahajnah, Muhammad
utue.personen.roh	Thomas, Mervyn G.
utue.personen.roh	Cohen, Yuval
utue.personen.roh	Habib, Adib
utue.personen.roh	Schulze, Martin
utue.personen.roh	Maconachie, Gail D. E.
utue.personen.roh	AlMoallem, Basamat
utue.personen.roh	De Baere, Elfride
utue.personen.roh	Lorenz, Birgit
utue.personen.roh	Traboulsi, Elias, I
utue.personen.roh	Kohl, Susanne
utue.personen.roh	Azem, Abdussalam
utue.personen.roh	Bauer, Peter
utue.personen.roh	Gottlob, Irene
utue.personen.roh	Sharkia, Rajech
utue.personen.roh	Wissinger, Bernd
dcterms.isPartOf.ZSTitelID	Brain	de_DE
dcterms.isPartOf.ZS-Volume	142	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE