FGF23 and its role in X-linked hypophosphatemia-related morbidity

BACKGROUND: X-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which inactivating mutations of the Phosphate Regulating Endopeptidase Homolog, X-Linked (PHEX) gene lead to local and systemic effects including impaired growth, rickets, osteomalacia, bone abnormalities,...

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Detalles Bibliográficos
Autores principales: Beck-Nielsen, Signe Sparre, Mughal, Zulf, Haffner, Dieter, Nilsson, Ola, Levtchenko, Elena, Ariceta, Gema, de Lucas Collantes, Carmen, Schnabel, Dirk, Jandhyala, Ravi, Mäkitie, Outi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390548/
https://www.ncbi.nlm.nih.gov/pubmed/30808384
http://dx.doi.org/10.1186/s13023-019-1014-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390548/
https://www.ncbi.nlm.nih.gov/pubmed/30808384
http://dx.doi.org/10.1186/s13023-019-1014-8

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