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Dental malformations associated with biallelic MMP20 mutations

dc.contributor.authorKasımoğlu, Yelda
dc.contributor.authorWang, Shih-Kai
dc.contributor.authorZhang, Hong
dc.contributor.authorChavez, Michael B.
dc.contributor.authorHu, Yuanyuan
dc.contributor.authorKoruyucu, Mine
dc.contributor.authorColvin, Connor D.
dc.contributor.authorKolli, Tamara N.
dc.contributor.authorTan, Michelle H.
dc.contributor.authorWang, Yin-Lin
dc.contributor.authorLu, Pei-Ying
dc.contributor.authorKim, Jung-Wook
dc.contributor.authorFoster, Brian L.
dc.contributor.authorBartlett, John D.
dc.contributor.authorSimmer, James P.
dc.contributor.authorHu, Jan C-C
dc.contributor.authorSeymen, Figen
dc.date.accessioned2021-03-02T18:14:12Z
dc.date.available2021-03-02T18:14:12Z
dc.identifier.citationWang S., Zhang H., Chavez M. B. , Hu Y., Seymen F., Koruyucu M., Kasımoğlu Y., Colvin C. D. , Kolli T. N. , Tan M. H. , et al., "Dental malformations associated with biallelic MMP20 mutations", MOLECULAR GENETICS & GENOMIC MEDICINE, 2020
dc.identifier.issn2324-9269
dc.identifier.otherav_271c236f-0e63-4b8c-bc4b-1f102facb4b8
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/4739
dc.identifier.urihttps://doi.org/10.1002/mgg3.1307
dc.description.abstractBackground Matrix metallopeptidase 20 (MMP20) is an evolutionarily conserved protease that is essential for processing enamel matrix proteins during dental enamel formation. MMP20 mutations cause human autosomal recessive pigmented hypomaturation-type amelogenesis imperfecta (AI2A2; OMIM #612529). MMP20 is expressed in both odontoblasts and ameloblasts, but its function during dentinogenesis is unclear.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectDahili Tıp Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.titleDental malformations associated with biallelic MMP20 mutations
dc.typeMakale
dc.relation.journalMOLECULAR GENETICS & GENOMIC MEDICINE
dc.contributor.departmentUniversity of Michigan System , ,
dc.contributor.firstauthorID2260544


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