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Mutations in CDK5RAP2 cause Seckel syndrome.

dc.contributor.authorRAUCH, A
dc.contributor.authorYIGIT, Günnur
dc.contributor.authorWOLLNIK, B
dc.contributor.authorROSSER, E
dc.contributor.authorBÖGERSHAUSEN, N
dc.contributor.authorLI, Y
dc.contributor.authorNÜRNBERG, G
dc.contributor.authorNÜRNBERG, P
dc.contributor.authorTHIEL, CT
dc.contributor.authorAltunoglu, UMUT
dc.contributor.authorUYGUNER, Zehra Oya
dc.contributor.authorBROWN, KE
dc.contributor.authorKAYSERILI, H
dc.contributor.authorPOHL, E
dc.contributor.authorCALIEBE, A
dc.contributor.authorZAHNLEITER, D
dc.date.accessioned2021-03-04T18:54:51Z
dc.date.available2021-03-04T18:54:51Z
dc.identifier.citationYIGIT G., BROWN K., KAYSERILI H., POHL E., CALIEBE A., ZAHNLEITER D., ROSSER E., BÖGERSHAUSEN N., UYGUNER Z. O. , Altunoglu U., et al., "Mutations in CDK5RAP2 cause Seckel syndrome.", Molecular genetics & genomic medicine, cilt.3, ss.467-80, 2015
dc.identifier.issn2324-9269
dc.identifier.otherav_8d2e7711-e5e7-467a-9c00-35a02bc8f62d
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/95448
dc.identifier.urihttps://doi.org/10.1002/mgg3.158
dc.language.isoeng
dc.titleMutations in CDK5RAP2 cause Seckel syndrome.
dc.typeMakale
dc.relation.journalMolecular genetics & genomic medicine
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri
dc.identifier.volume3
dc.identifier.startpage467
dc.identifier.endpage80
dc.contributor.firstauthorID182256


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