| dc.contributor.author | Puente Ruiz, Nuria | |
| dc.contributor.author | Solis, Pablo | |
| dc.contributor.author | Riancho Moral, José Antonio | |
| dc.contributor.other | Universidad de Cantabria | es_ES |
| dc.date.accessioned | 2025-03-25T18:22:42Z | |
| dc.date.available | 2025-03-25T18:22:42Z | |
| dc.date.issued | 2024 | |
| dc.identifier.issn | 0026-4806 | |
| dc.identifier.issn | 1827-1669 | |
| dc.identifier.uri | https://hdl.handle.net/10902/36093 | |
| dc.description.abstract | Phosphate is a key component of mineralized tissues and is also part of many organic compounds. Phosphorus homeostasis depends especially upon intestinal absorption, and renal excretion, which are regulated by various hormones, such as PTH, 1,25-dihydroxyvitamin D, and fibroblast growth factor 23. In this review we provide an update of several genetic disorders that affect phosphate transporters through cell membranes or the phosphate-regulating hormones, and, consequently, result in hypophosphatemia. | es_ES |
| dc.format.extent | 26 p. | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | Edizioni Minerva Medica | es_ES |
| dc.rights | © 2024 Edizioni Minerva Medica | es_ES |
| dc.source | Minerva Medica, 2024, 115(3), 320-336 | es_ES |
| dc.subject.other | Hypophosphatemia | es_ES |
| dc.subject.other | Genetics | es_ES |
| dc.subject.other | Fibroblast growth factor 23 | es_ES |
| dc.subject.other | Rickets | es_ES |
| dc.subject.other | Osteomalacia | es_ES |
| dc.title | Genetic causes of hypophosphatemia | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.rights.accessRights | openAccess | es_ES |
| dc.identifier.DOI | 10.23736/S0026-4806.24.09198-5 | |
| dc.type.version | acceptedVersion | es_ES |
