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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...

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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

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