Targeted resequencing of phosphorus metabolism‑related genes in 86 patients with hypophosphatemic rickets/osteomalacia
Author:
Affiliation:
1. Metabolic Bone Disease and Genetic Research Unit, Department of Osteoporosis and Bone Diseases, Shanghai Key Clinical Center for Metabolic Disease, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, P.R. China
Publisher
Spandidos Publications
Subject
Genetics,General Medicine
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Identification of six novel variants from nine Chinese families with hypophosphatemic rickets;BMC Medical Genomics;2022-07-16
2. Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study;Pediatric Nephrology;2022-01-10
3. Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults;Endokrynologia Polska;2021-08-11
4. Identification of low-frequency variants of UGT1A3 associated with bladder cancer risk by next-generation sequencing;Oncogene;2021-03-03
5. Clinical Characteristics and Bone Features of Autosomal Recessive Hypophosphatemic Rickets Type 1 in Three Chinese Families: Report of Five Chinese Cases and Review of the Literature;Calcified Tissue International;2020-09-12
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