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Pathogenic role of Fgf23 in Dmp1-null mice

Autosomal recessive hypophosphatemic rickets (ARHR), which is characterized by renal phosphate wasting, aberrant regulation of 1α-hydroxylase activity, and rickets/osteomalacia, is caused by inactivating mutations of dentin matrix protein 1 (DMP1). ARHR resembles autosomal dominant hypophosphatemic...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Liu, Shiguang, Zhou, Jianping, Tang, Wen, Menard, Rochelle, Feng, Jian Q., Quarles, L. D.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Physiological Society 2008
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2519751/
https://ncbi.nlm.nih.gov/pubmed/18559986
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpendo.90201.2008
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