Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults
Hypophosphataemic rickets (HR) is a genetic disorder causing defects in the renal handling of phosphorus, resulting in rickets. HR can be classified into two groups. First- those with excess fibroblast growth factor 23(FGF23) levels, which are due to gene mutations in extrarenal factors and include...
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| Main Authors: | , , , |
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| Format: | Article |
| Published: |
Via Medica
2021
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| Online Access: | http://psasir.upm.edu.my/id/eprint/96184/ https://journals.viamedica.pl/endokrynologia_polska/article/view/72827 |
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| Institution: | Universiti Putra Malaysia |