reference/23043053

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endingPage	1206
issn	1523-4681 0884-0431
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pageRange	1200-1206
publicationName	Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
startingPage	1200
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bibliographicCitation	Gorvin CM, Cranston T, Hannan FM, Rust N, Qureshi A, Nesbit MA, Thakker RV. 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. PMID: 26729423; PMCID: PMC4949650.
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date	2016-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/jbmr.2778 https://pubmed.ncbi.nlm.nih.gov/PMC4949650 https://pubmed.ncbi.nlm.nih.gov/26729423
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)
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