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hyperparathyroidism
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CASR
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
Mapping of the calcium-sensing receptor gene (CASR) to human chromosome 3q13.3-21 by fluorescence in situ hybridization, and localization to rat chromosome 11 and mouse chromosome 16
Changes in calcium responsiveness and handling during keratinocyte differentiation. Potential role of the calcium receptor
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism
Expression and characterization of inactivating and activating mutations in the human Ca2+o-sensing receptor
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Class C/3 (Metabotropic glutamate/pheromone receptors)
species not specified
one gene
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Studies of Inherited Diseases of Metabolism