Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

Amelogenesis imperfecta is a group of rare inherited disorders that affect tooth enamel formation, quantitatively and/or qualitatively. The aim of this study was to identify the genetic etiologies of two families presenting with hypomaturation amelogenesis imperfecta. DNA was isolated from periphera...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Physiol
Prif Awduron: Kim, Youn Jung, Kang, Jenny, Seymen, Figen, Koruyucu, Mine, Gencay, Koray, Shin, Teo Jeon, Hyun, Hong-Keun, Lee, Zang Hee, Hu, Jan C.-C., Simmer, James P., Kim, Jung-Wook
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2017
Pynciau:
Physiology
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5397402/
https://ncbi.nlm.nih.gov/pubmed/28473773
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2017.00229
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