A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome (vol 132, pg 1311, 2013)

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dc.contributor.authorPohl, Esther
dc.contributor.authorAykut, Ayca
dc.contributor.authorBeleggia, Filippo
dc.contributor.authorKaraca, Emin
dc.contributor.authorDurmaz, Burak
dc.contributor.authorKeupp, Katharina
dc.contributor.authorArslan, Esra
dc.contributor.authorPalamar, Melis
dc.contributor.authorYigit, Goekhan
dc.contributor.authorÖzkınay, Ferda
dc.contributor.authorWollnik, Bernd
dc.date.accessioned2019-10-27T22:07:25Z
dc.date.available2019-10-27T22:07:25Z
dc.date.issued2013
dc.departmentEge Üniversitesien_US
dc.identifier.doi10.1007/s00439-013-1341-0
dc.identifier.endpage1321en_US
dc.identifier.issn0340-6717
dc.identifier.issn1432-1203
dc.identifier.issue11en_US
dc.identifier.startpage1321en_US
dc.identifier.urihttps://doi.org/10.1007/s00439-013-1341-0
dc.identifier.urihttps://hdl.handle.net/11454/49009
dc.identifier.volume132en_US
dc.identifier.wosWOS:000325706500012en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofHuman Geneticsen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleA hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome (vol 132, pg 1311, 2013)en_US
dc.typeOtheren_US

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