Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

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dc.contributor.author Kohl, Susanne de_DE
dc.date.accessioned 2013-07-22T11:14:19Z
dc.date.available 2013-07-22T11:14:19Z
dc.date.issued 2013 de_DE
dc.identifier.issn 0002-9297 de_DE
dc.identifier.uri http://hdl.handle.net/10900/36194
dc.language.iso en en
dc.publisher Cell Press de_DE
dc.relation.uri http://dx.doi.org/10.1016/j.ajhg.2012.10.023 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness de_DE
dc.type Article de_DE
utue.quellen.id 20130315161744_00234 de_DE
utue.publikation.seiten 67-75 de_DE
utue.personen.roh Zeitz, Christina de_DE
utue.personen.roh Jacobson, Samuel G. de_DE
utue.personen.roh Hamel, Christian P. de_DE
utue.personen.roh Bujakowska, Kinga de_DE
utue.personen.roh Neuille, Marion de_DE
utue.personen.roh Orhan, Elise de_DE
utue.personen.roh Zanlonghi, Xavier de_DE
utue.personen.roh Lancelot, Marie-Elise de_DE
utue.personen.roh Michiels, Christelle de_DE
utue.personen.roh Schwartz, Sharon B. de_DE
utue.personen.roh Bocquet, Beatrice de_DE
utue.personen.roh Antonio, Aline de_DE
utue.personen.roh Audier, Claire de_DE
utue.personen.roh Letexier, Melanie de_DE
utue.personen.roh Saraiva, Jean-Paul de_DE
utue.personen.roh Luu, Tien D. de_DE
utue.personen.roh Sennlaub, Florian de_DE
utue.personen.roh Nguyen, Hoan de_DE
utue.personen.roh Poch, Olivier de_DE
utue.personen.roh Dollfus, Helene de_DE
utue.personen.roh Lecompte, Odile de_DE
utue.personen.roh Kohl, Susanne de_DE
utue.personen.roh Sahel, Jose-Alain de_DE
utue.personen.roh Bhattacharya, Shomi S. de_DE
utue.personen.roh Audo, Isabelle de_DE
dcterms.isPartOf.ZSTitelID American Journal of Human Genetics de_DE
dcterms.isPartOf.ZS-Issue 1 de_DE
dcterms.isPartOf.ZS-Volume 92 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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