MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta

The Amelogenesis Imperfecta (AI) are a group of clinically and genetically heterogeneous disorders that affect enamel formation. To date, mutations in 4 genes have been reported in various types of AI. Mutations in the genes encoding the 2 enamel proteases, matrix metalloproteinase 20 (MMP20) and ka...

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Autores principales: Ozdemir, D., Hart, P.S., Ryu, O.H., Choi, S.J., Ozdemir-Karatas, M., Firatli, E., Piesco, N., Hart, T.C.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2005
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1850238/
https://ncbi.nlm.nih.gov/pubmed/16246936
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