A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities

“Amelogenesis imperfecta” (AI) describes a group of genetic conditions that result in defects in tooth enamel formation. Mutations in many genes are known to cause AI, including the gene encoding the serine protease, kallikrein related peptidase 4 (KLK4), expressed during the maturation stage of ame...

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Detalles Bibliográficos
Autores principales: Smith, Claire E. L., Kirkham, Jennifer, Day, Peter F., Soldani, Francesca, McDerra, Esther J., Poulter, James A., Inglehearn, Christopher F., Mighell, Alan J., Brookes, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447068/
https://www.ncbi.nlm.nih.gov/pubmed/28611678
http://dx.doi.org/10.3389/fphys.2017.00333

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447068/
https://www.ncbi.nlm.nih.gov/pubmed/28611678
http://dx.doi.org/10.3389/fphys.2017.00333

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