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

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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


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