Fa-Qiang Tang
4PUBLICATIONS
24CO-AUTHORS
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Publications (4)
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|Jun 02, 2022
Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.Yu-Mian Gan, Yan-Ping Zhang, Dan-Dan Ruan
|Apr 05, 2022
Prevalence, Risk Factors, and Prognostic Factors of Primary Malignant Bone Neoplasms with Bone Metastasis at Initial Diagnosis: A Population-Based Study.Zheng-Wei Xiao, Hui-Ling Guo, Hong-Chao Chen
|Nov 16, 2021
Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.Wen Wei, Xiu-Fen Zheng, Dan-Dan Ruan
|May 28, 2021
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.Jian-Hui Zhang, Dan-Dan Ruan, Ya-Nan Hu
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Frequent Collaborators
3 joint publications
Jie-Wei Luo
2 joint publications
Dan-Dan Ruan
2 joint publications
Xin-Fu Lin
2 joint publications
Yu-Mian Gan
1 joint publications
Jian-Hui Zhang
1 joint publications
Ya-Nan Hu
1 joint publications
Xing-Lin Ruan
1 joint publications
Yao-Bin Zhu
1 joint publications
Xiao Yang
1 joint publications
Jia-Bin Wu
