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Identification of Two Novel Mutations in the PHEX Gene in Chinese Patients with Hypophosphatemic Rickets/Osteomalacia

  • Published:2014-05-16 Issue:5 Volume:9 Page:e97830
  • ISSN:1932-6203
  • Container-title:PLoS ONE
  • language:en
  • Short-container-title:PLoS ONE

Author:

Yue Hua,Yu Jin-bo,He Jin-wei,Zhang Zeng,Fu Wen-zhen,Zhang Hao,Wang Chun,Hu Wei-wei,Gu Jie-mei,Hu Yun-qiu,Li Miao,Liu Yu-juan,Zhang Zhen-Lin

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference30 articles.

1. Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia;PS Rowe;Hum Genet,1994

2. Distribution of mutations in the PHEX gene in families with X-linked hypophosphataemic rickets (HYP);PS Rowe;Hum Mol Genet,1997

3. The role of the PHEX gene (PEX) in families with X-linked hypophosphataemic rickets;PS Rowe;Curr Opin Nephrol Hypertens,1998

4. Pathophysiology of X-linked hypophosphatemia, tumor-induced osteomalacia, and autosomal dominant hypophosphatemia: a perPHEXing problem;LD Quarles;J Clin Endocrinol Metab,2001

5. Rickets resistant to vitamin D therapy;F Albright;American Journal of Disease of Children,1939

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