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PubMed (cited) for id: 145981
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A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2).
J Bone Miner Res. 2016 Jun;31(6):1200-6. doi: 10.1002/jbmr.2778. Epub 2016 Feb 6.
J Bone Miner Res. 2016.
PMID: 26729423
Free PMC article.
Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia.
Nesbit MA, Hannan FM, Howles SA, Babinsky VN, Head RA, Cranston T, Rust N, Hobbs MR, Heath H 3rd, Thakker RV.
Nesbit MA, et al.
N Engl J Med. 2013 Jun 27;368(26):2476-2486. doi: 10.1056/NEJMoa1300253.
N Engl J Med. 2013.
PMID: 23802516
Free PMC article.
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Genetic linkage analysis in familial benign hypercalcemia using a candidate gene strategy. I. Studies in four families.
Heath H 3rd, Leppert MF, Lifton RP, Penniston JT.
Heath H 3rd, et al.
J Clin Endocrinol Metab. 1992 Sep;75(3):846-51. doi: 10.1210/jcem.75.3.1517376.
J Clin Endocrinol Metab. 1992.
PMID: 1517376
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