Genetica dell’ipercalcemia ipocalciurica familiare
Author:
Publisher
Springer Science and Business Media LLC
Subject
Microbiology
Link
https://link.springer.com/content/pdf/10.1007/s40619-023-01336-0.pdf
Reference7 articles.
1. Vahe C, Benomar K, Espiard S et al. (2017) Diseases associated with calcium-sensing receptor. Orphanet J Rare Dis 12:19
2. Hendy GN, Guarnieri V, Canaff L (2009) Calcium-sensing receptor and associated diseases. Prog Mol Biol Transl Sci 89:31–95
3. Nesbit MA, Hannan FM, Howles SA et al. (2013) Mutations affecting G-protein subunit $\alpha $11 in hypercalcemia and hypocalcemia. N Engl J Med 368:2476–2486
4. Nesbit MA, Hannan FM, Howles SA et al. (2013) Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3. Nat Genet 45:93–97
5. Vargas-Poussou R, Mansour-Hendili L, Baron S et al. (2016) Familial hypocalciuric hypercalcemia types 1 and 3 and primary hyperparathyroidism: similarities and differences. J Clin Endocrinol Metab 101:2185–2195
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