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In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.
Bai M, Pearce SH, Kifor O, Trivedi S, Stauffer UG, Thakker RV, Brown EM, Steinmann B. Bai M, et al. J Clin Invest. 1997 Jan 1;99(1):88-96. doi: 10.1172/JCI119137. J Clin Invest. 1997. PMID: 9011580 Free PMC article.
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