Dental malformations associated with biallelic MMP20 mutations

BACKGROUND: 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)....

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Detalles Bibliográficos
Autores principales: Wang, Shih‐Kai, Zhang, Hong, Chavez, Michael B., Hu, Yuanyuan, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Colvin, Connor D., Kolli, Tamara N., Tan, Michelle H., Wang, Yin‐Lin, Lu, Pei‐Ying, Kim, Jung‐Wook, Foster, Brian L., Bartlett, John D., Simmer, James P., Hu, Jan C.‐C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434610/
https://www.ncbi.nlm.nih.gov/pubmed/32495503
http://dx.doi.org/10.1002/mgg3.1307

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