X-linked hypophosphatemic rickets: an Italian experts' opinion survey

X-linked hypophosphatemic rickets: an Italian experts' opinion survey

Abstract Background X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia and is caused by mutation in the PHEX gene, resulting in excessive expression of the phosphaturic factor FGF23. Symptoms are mainly related to rickets in children and osteomalacia in adults a...

Full description

Saved in:
Bibliographic Details
Main Authors: F. Emma (Author), M. Cappa (Author), F. Antoniazzi (Author), M. L. Bianchi (Author), I. Chiodini (Author), C. Eller Vainicher (Author), N. Di Iorgi (Author), M. Maghnie (Author), A. Cassio (Author), A. Balsamo (Author), F. Baronio (Author), L. de Sanctis (Author), D. Tessaris (Author), G. I. Baroncelli (Author), S. Mora (Author), M. L. Brandi (Author), G. Weber (Author), A. D'Ausilio (Author), E. P. Lanati (Author)
Format: Book
Published: BMC, 2019-05-01T00:00:00Z.
Subjects:
article
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available

Similar Items