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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: 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.
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 2011
Fag:
PNAS Plus
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker