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Standards and guidelines for the interpretation of sequence variants: a            joint consensus recommendation of the American College of Medical Genetics and Genomics            and the Association for Molecular Pathology. Genet Med          2015;17: 405\u201324.","DOI":"10.1038\/gim.2015.30"},{"key":"4","doi-asserted-by":"publisher","unstructured":"4. Shimada,              T, Muto,                T, Urakawa,                I, Yoneya,                T,              Yamazaki, Y,                Okawa, K,              et al. Mutant FGF-23 responsible for            autosomal dominant hypophosphatemic rickets is resistant to proteolytic cleavage and            causes hypophosphatemia in vivo. Endocrinology          2002;143: 3179\u201382.","DOI":"10.1210\/en.143.8.3179"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Econs,              MJ, McEnery,                PT. Autosomal            dominant hypophosphatemic rickets\/osteomalacia: clinical characterization of a novel            renal phosphate-wasting disorder. J Clin Endocrinol            Metab          1997;82: 674\u201381.","DOI":"10.1210\/jcem.82.2.3765"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Imel,              EA, Liu,                Z, Coffman,                M, Acton,                D, Mehta,                R, Econs,                MJ. Oral iron            replacement normalizes fibroblast growth factor 23 in iron-deficient patients with            autosomal dominant hypophosphatemic rickets. J Bone Miner            Res          2020;35: 231\u20138.","DOI":"10.1002\/jbmr.3878"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Imel,              EA, Peacock,                M, Gray,                AK,              Padgett, LR,                Hui, SL,                Econs,            MJ. 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