New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT). [electronic resource]

By: Contributor(s): Producer: 20111024Description: 67-71 p. digitalISSN:
  • 1677-9487
Subject(s): Online resources: In: Arquivos brasileiros de endocrinologia e metabologia vol. 55
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Publication Type: Case Reports; Journal Article

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