Daina Dreimane
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0CO-AUTHORS

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Publications (1)
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|Sep 23, 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
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