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  • Molecular assay reagents intended to identify mutations in the calcium sensing receptor (CASR) gene, located at chromosome 3q13, which encodes the protein extracellular calcium-sensing receptor. Genetic variants at this locus have been associated with idiopathic generalized epilepsy 8, familial hypocalciuric hypercalcemia type 1, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia 1.
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