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Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains.

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Year: 1996
Type: article
Study design: Observational Study
Source: The Journal of Clinical Endocrinology & Metabolism
DOI: 10.1210/jcem.81.4.8636323
Authors: H Heath, S Odelberg, C E Jackson, B T Teh, N Hayward, C Larsson, N R Buist, K J Krapcho, B C Hung, I V Capuano, J E Garrett, M F Leppert
Institution: University of Utah
Language: English

Topic: Parathyroid Disorders and Treatments
Subfield: Nephrology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Human Genome Research Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources
Awards: G2392299489, G284809622, TOOLS FOR HIGH RESOLUTION LINKAGE MAPPING OF HUMAN GENES, G495555665, PATHOGENESIS OF HYPERCALCEMIA, General Clinical Research Center
OpenAlex ID: W2157138210
FWCI: 15.37
Cites: 35
Cited by: 182
Related to: 10
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