Functional Characterization of PHEX Gene Variants in Children With X ‐Linked Hypophosphatemic Rickets Shows No Evidence of Genotype–Phenotype Correlation-Reference-Cited by-同舟云学术

Functional Characterization of PHEX Gene Variants in Children With X ‐Linked Hypophosphatemic Rickets Shows No Evidence of Genotype–Phenotype Correlation

Published:2020-05-12 Issue:9 Volume:35 Page:1718-1725
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Zheng Bixia¹,Wang Chunli¹,Chen Qiuxia²,Che Ruochen²,Sha Yugen²,Zhao Fei²,Ding Guixia²,Zhou Wei¹,Jia Zhanjun¹,Huang Songming²³,Chen Ying²,Zhang Aihua²³^ORCID

Affiliation:

1. Nanjing Key Laboratory of Pediatrics Children's Hospital of Nanjing Medical University Nanjing China

2. Department of Nephrology Children's Hospital of Nanjing Medical University Nanjing China

3. Jiangsu Key Laboratory of Pediatrics Nanjing Medical University Nanjing China

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbmr.4035

Reference31 articles.

1. Hypophosphatemic rickets: etiology, clinical features and treatment