Associated Papers
Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta.
Lee Y et al.
Journal of Personalized Medicine, 2022
Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta.
Yoshioka H et al.
International Journal of Molecular Sciences, 2021
33672174 (PubMed )
Supplement: ijms-22-02202-s001.zip › Supplementary_Table_S4-1_Final_021921.xlsx › Table_S3.1
A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities.
Smith CEL et al.
Frontiers in Physiology, 2017
Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.
Seymen F et al.
Journal of Dental Research, 2015
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