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Medicine Health Nutrition Vitamin D Electrolyte disturbances Rare diseases Skeletal disorders Solute carrier family Autosomal dominant hypophosphatemic rickets Fibroblast growth factor 23 SLC34A3 Hypophosphatemia | NIH Public Access Author Manuscript Bone. Author manuscript; available in PMC 2013 May 1. NIH-PA Author ManuscriptAdd to Reading ListSource URL: www.ncbi.nlm.nih.govDownload Document from Source WebsiteFile Size: 837,25 KBShare Document on Facebook |
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