{"id":"W2137591192","doi":"10.1073/pnas.1110905108","title":"Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice","year":2011,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Parathyroid Disorders and Treatments","field":"Medicine","cited_by":381,"is_retracted":false,"has_abstract":true,"ca_institutions":"","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institutes of Health; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; University of Ottawa; Lilly Endowment; Indiana Clinical and Translational Sciences Institute; Eli Lilly and Company","keywords":"Hypophosphatemic Rickets; PHEX; Osteomalacia; Fibroblast growth factor 23; Endocrinology; Rickets; Internal medicine; Hypophosphatemia; Iron deficiency; Chemistry; Medicine; Calcium; Anemia; Vitamin D and neurology; Parathyroid hormone","routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":true},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.04168474980859135,"score_gpt":0.2958159935658234,"score_spread":0.2541312437572321,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}