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Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)<sub>2</sub>D serum levels are associated with <it>PHEX </it>mutation type
García-Miñaur Sixto, García-Sagredo José M, Soriano-Guillén Leandro and 26 more
BMC Medical Genetics · 2011
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