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Select article: Description of a novel SLC34A3.c.671delT mutation causing hereditary hypophosphatemic rickets with hypercalciuria in two adolescent boys and response to recombinant human growth hormone

Open access

Case report

First published 2020

Description of a novel SLC34A3.c.671delT mutation causing hereditary hypophosphatemic rickets with hypercalciuria in two adolescent boys and response to recombinant human growth hormone

Daina Dreimane, Alyssa Chen, Clemens Bergwitz

Therapeutic Advances in Musculoskeletal Disease

Select article: Pleiotropic Actions of FGF23

Open access

Research article

First published October, 2017

Pleiotropic Actions of FGF23

Reinhold G. Erben

Toxicologic Pathology

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