DMP1 C-Terminal Mutant Mice Recapture the Human ARHR Tooth Phenotype

DMP1 mutations in autosomal recessive hypophosphatemic rickets (ARHR) patients and mice lacking Dmp1 display an overlapping pathophysiology, such as hypophosphatemia. However, subtle differences exist between the mouse model and human ARHR patients. These differences could be due to a species specif...

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Detalles Bibliográficos
Autores principales: Jiang, Baichun, Cao, Zhengguo, Lu, Yongbo, Janik, Carol, Lauziere, Stephanie, Xie, Yixia, Poliard, Anne, Qin, Chunlin, Ward, Leanne M, Feng, Jian Q
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153318/
https://www.ncbi.nlm.nih.gov/pubmed/20499360
http://dx.doi.org/10.1002/jbmr.117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153318/
https://www.ncbi.nlm.nih.gov/pubmed/20499360
http://dx.doi.org/10.1002/jbmr.117

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