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pubmed-article:21050253pubmed:abstractTextX-linked hypophosphatemic rickets, autosomal dominant hypophosphatemic rickets and autosomal recessive hypophosphatemic rickets make up a group of renal phosphate wasting disorders with common clinical and biochemical characteristics. These three types of rickets are related to mutations in PHEX, FGF23 and dentin matrix protein 1 (DMP1), respectively.lld:pubmed
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pubmed-article:21050253pubmed:articleTitleMutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets.lld:pubmed
pubmed-article:21050253pubmed:affiliationDepartment of Medicine, University of Texas Health Science Center at Houston, TX 77030, USA. mary.ruppe@uth.tmc.edulld:pubmed
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