Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta

dc.contributor.author	Kım, Y-J
dc.contributor.author	Hyun, H-K
dc.contributor.author	Shın, T. J.
dc.contributor.author	Lee, Z. H.
dc.contributor.author	Kım, J-W
dc.contributor.author	Kasimoglu, Y.
dc.contributor.author	Koruyucu, M.
dc.contributor.author	Gencay, K.
dc.contributor.author	Seymen, Figen
dc.date.accessioned	2020-09-02T06:58:16Z
dc.date.available	2020-09-02T06:58:16Z
dc.date.issued	2016
dc.identifier.citation	Kım Y., Seymen F., Koruyucu M., Kasimoglu Y., Gencay K., Shın T. J. , Hyun H., Lee Z. H. , Kım J., "Unexpected İdentification Of A Recurrent Mutation İn The Dlx3 Gene Causing Amelogenesis İmperfecta", Oral Dıseases, Vol.22, Pp.297-302, 2016
dc.identifier.issn	1354-523X
dc.identifier.uri	10.1111/odi.12439
dc.identifier.uri	http://hdl.handle.net/20.500.12627/1050
dc.description.abstract	ObjectiveTo identify the molecular genetic aetiology of a family with autosomal dominant amelogenesis imperfecta (AI).
dc.language.iso	eng
dc.rights	Atıf 4.0 Uluslararası
dc.rights.uri	info:eu-repo/semantics/openAccess
dc.rights.uri	http://creativecommons.org/licenses/by/4.0/
dc.subject	Dentıstry, Oral Surgery & Medıcıne
dc.title	Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta
dc.type	article
dc.contributor.department	Diş Hekimliği Fakültesi,Pedodonti,Pedodonti
dc.contributor.authorID	0000-0001-7010-2035
dc.identifier.volume	22
dc.identifier.issue	4
dc.identifier.startpage	297
dc.identifier.endpage	302

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