SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss

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dc.contributor.author Buchert, Rebecca
dc.date.accessioned 2018-11-27T08:26:35Z
dc.date.available 2018-11-27T08:26:35Z
dc.date.issued 2016
dc.identifier.issn 1750-1172
dc.identifier.uri http://hdl.handle.net/10900/84989
dc.language.iso en de_DE
dc.publisher Biomed Central Ltd de_DE
dc.relation.uri http://dx.doi.org/10.1186/s13023-016-0509-9 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss de_DE
dc.type Artikel de_DE
utue.quellen.id 20180405102126_01096
utue.personen.roh Buchert, Rebecca
utue.personen.roh Nesbitt, Addie I.
utue.personen.roh Tawamie, Hasan
utue.personen.roh Krantz, Ian D.
utue.personen.roh Medne, Livija
utue.personen.roh Helbig, Ingo
utue.personen.roh Matalon, Dena R.
utue.personen.roh Reis, Andre
utue.personen.roh Santani, Avni
utue.personen.roh Sticht, Heinrich
utue.personen.roh Abou Jamra, Rami
dcterms.isPartOf.ZSTitelID Orphanet Journal of Rare Diseases de_DE
dcterms.isPartOf.ZS-Issue Article 130 de_DE
dcterms.isPartOf.ZS-Volume 11 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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