Genetic analysis combined with 3D‐printing assistant surgery in diagnosis and treatment for an X‐linked hypophosphatemia patient-Reference-Cited by-同舟云学术

Genetic analysis combined with 3D‐printing assistant surgery in diagnosis and treatment for an X‐linked hypophosphatemia patient

Published:2022-02-02 Issue:3 Volume:36 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:Clinical Laboratory Analysis

Author:

Jin Jie‐Yuan¹²³,Zhang Li‐Yang⁴⁵,Guo Shuai²,Tang Ke²³⁵,Zeng Lei¹⁵,Xiang Rong¹²³⁵^ORCID,Liang Jie‐Yu¹⁵^ORCID

Affiliation:

1. Department of Orthopaedics Xiangya Hospital of Central South University Changsha China

2. School of Life Sciences Central South University Changsha China

3. Hunan Key Laboratory of Animal Models for Human Diseases Central South University Changsha China

4. Department of Neurosurgery Xiangya Hospital Central South University Changsha China

5. Hunan Key Laboratory of Medical Genetics School of Life Sciences Central South University Changsha China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.24243

Reference19 articles.

1. X-Linked Hypophosphatemia and FGF23-Related Hypophosphatemic Diseases: Prospect for New Treatment

2. Familial hypophosphatemic rickets caused by a large deletion in PHEX gene

3. Human Fibroblast Growth Factor-23 Mutants Suppress Na+-dependent Phosphate Co-transport Activity and 1α,25-Dihydroxyvitamin D3 Production

4. Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism

5. Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets

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