Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta

OBJECTIVE: Hereditary defects in tooth enamel formation, amelogenesis imperfecta (AI), can be non-syndromic or syndromic phenotype. Integrins are signaling proteins that mediate cell–cell and cell–extracellular matrix communication, and their involvement in tooth development is well known. The purpo...

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Detalles Bibliográficos
Autores principales: Seymen, F, Lee, K-E, Koruyucu, M, Gencay, K, Bayram, M, Tuna, EB, Lee, ZH, Kim, J-W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440386/
https://www.ncbi.nlm.nih.gov/pubmed/25431241
http://dx.doi.org/10.1111/odi.12303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440386/
https://www.ncbi.nlm.nih.gov/pubmed/25431241
http://dx.doi.org/10.1111/odi.12303

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