Enamel defects in Acp4(R110C/R110C) mice and human ACP4 mutations

Human ACP4 (OMIM*606362) encodes a transmembrane protein that belongs to histidine acid phosphatase (ACP) family. Recessive mutations in ACP4 cause non-syndromic hypoplastic amelogenesis imperfecta (AI1J, OMIM#617297). While ACP activity has long been detected in developing teeth, its functions duri...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Tian, Wang, Shih-Kai, Smith, Charles, Zhang, Hong, Hu, Yuanyuan, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Kim, Jung-Wook, Zhang, Chuhua, Saunders, Thomas L., Simmer, James P., Hu, Jan C.-C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526733/
https://www.ncbi.nlm.nih.gov/pubmed/36183038
http://dx.doi.org/10.1038/s41598-022-20684-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526733/
https://www.ncbi.nlm.nih.gov/pubmed/36183038
http://dx.doi.org/10.1038/s41598-022-20684-9

Ejemplares similares