The Autosomal Dominant Hypophosphatemic Rickets R176Q Mutation in Fibroblast Growth Factor 23 Resists Proteolytic Cleavage and Enhances in Vivo Biological Potency-Reference-Cited by-同舟云学术

The Autosomal Dominant Hypophosphatemic Rickets R176Q Mutation in Fibroblast Growth Factor 23 Resists Proteolytic Cleavage and Enhances in Vivo Biological Potency

Published:2003-03 Issue:11 Volume:278 Page:9843-9849
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Bai Xiu-Ying,Miao Dengshun,Goltzman David,Karaplis Andrew C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference26 articles.

1. Autosomal Dominant Hypophosphatemic Rickets/Osteomalacia: Clinical Characterization of a Novel Renal Phosphate-Wasting Disorder

2. A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

3. Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP)

4. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

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