The Enamel Phenotype in Homozygous Fam83h Truncation Mice

BACKGROUND: Truncation FAM83H mutations cause human autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI), an inherited disorder characterized by severe hardness defects in dental enamel. No enamel defects were observed in Fam83h null mice suggesting that Fam83h truncation mice would bet...

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Detalles Bibliográficos
Autores principales: Wang, Shih‐Kai, Hu, Yuanyuan, Smith, Charles E., Yang, Jie, Zeng, Chunhua, Kim, Jung‐Wook, Hu, Jan C‐C., Simmer, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565571/
https://www.ncbi.nlm.nih.gov/pubmed/31060110
http://dx.doi.org/10.1002/mgg3.724

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565571/
https://www.ncbi.nlm.nih.gov/pubmed/31060110
http://dx.doi.org/10.1002/mgg3.724

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