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This page is a summary of: Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused byAP2S1Mutation, The Journal of Clinical Endocrinology & Metabolism, July 2015, Endocrine Society,
DOI: 10.1210/jc.2015-1518.
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