Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis Imperfecta

Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis Imperfecta

Amelogenesis imperfecta (AI) is a group of rare genetic diseases affecting the tooth enamel. AI is characterized by an inadequate quantity and/or quality of tooth enamel and can be divided into three major categories: hypoplastic, hypocalcified and hypomaturation types. Even though there are some ov...

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Bibliographic Details
Main Authors: Yejin Lee, Hong Zhang, Figen Seymen, Youn Jung Kim, Yelda Kasimoglu, Mine Koruyucu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:Journal of Personalized Medicine
Subjects:
whole exome sequencing
kallikrein 4
amelogenesis imperfecta
genetic diseases
hypomaturation
zymography
Online Access:https://www.mdpi.com/2075-4426/12/2/150

Internet

https://www.mdpi.com/2075-4426/12/2/150

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