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Three inherited disorders of calcium sensing.
The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.
Cloning and functional characterization of extracellular Ca(2+)-sensing receptors from parathyroid and kidney.
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
GENETICS OF FAMILIAL HYPOCALCIURIC HYPERCALCEMIA