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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Detalhes bibliográficos
Main Authors: Jiang, Baichun, Cao, Zhengguo, Lu, Yongbo, Janik, Carol, Lauziere, Stephanie, Xie, Yixia, Poliard, Anne, Qin, Chunlin, Ward, Leanne M, Feng, Jian Q
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Subscription Services, Inc., A Wiley Company 2010
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3153318/
https://ncbi.nlm.nih.gov/pubmed/20499360
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.117
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