Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice

Autosomal dominant hypophosphatemic rickets (ADHR) is unique among the disorders involving Fibroblast growth factor 23 (FGF23) because individuals with R176Q/W and R179Q/W mutations in the FGF23 (176)RXXR(179)/S(180) proteolytic cleavage motif can cycle from unaffected status to delayed onset of dis...

詳細記述

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書誌詳細
主要な著者: Farrow, Emily G., Yu, Xijie, Summers, Lelia J., Davis, Siobhan I., Fleet, James C., Allen, Matthew R., Robling, Alexander G., Stayrook, Keith R., Jideonwo, Victoria, Magers, Martin J., Garringer, Holly J., Vidal, Ruben, Chan, Rebecca J., Goodwin, Charles B., Hui, Siu L., Peacock, Munro, White, Kenneth E.
フォーマット: Artigo
言語:Inglês
出版事項: National Academy of Sciences 2011
主題:
PNAS Plus
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3219119/
https://ncbi.nlm.nih.gov/pubmed/22006328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1110905108
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