X-linked hypophosphatemia: a search for gender, race, anticipation, or parent of origin effects on disease expression in children
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 82 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. X-Linked hypophosphatemia. Data from a Spanish adult population cohort;Journal of Nephrology;2024-06-05
2. Lessons learned from the real-world diagnosis and management of hereditary hypophosphatemic rickets;Bone Reports;2024-06
3. The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model;Frontiers in Endocrinology;2023-12-05
4. X-Linked Familial Hypophosphatemia: A Case Report of 27-Year Old Male and Review of Literature;Hormone and Metabolic Research;2023-10
5. Osteomalacia hipofosfatémica ligada al cromosoma X (XLH): análisis de 5 pacientes adultos;Medicina Clínica;2023-03
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