FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting

FGF-23, a novel member of the FGF family, is the product of the gene mutated in autosomal dominant hypophosphatemic rickets (ADHR). FGF-23 has been proposed as a circulating factor causing renal phosphate wasting not only in ADHR (as a result of inadequate degradation), but also in tumor-induced ost...

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Detalhes bibliográficos
Main Authors: Riminucci, Mara, Collins, Michael T., Fedarko, Neal S., Cherman, Natasha, Corsi, Alessandro, White, Kenneth E., Waguespack, Steven, Gupta, Anurag, Hannon, Tamara, Econs, Michael J., Bianco, Paolo, Gehron Robey, Pamela
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2003
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC182207/
https://ncbi.nlm.nih.gov/pubmed/12952917
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200318399
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