A Woman and Her Father with Calcium-Sensing Receptor Mutation and Autosomal Dominant Hypocalcemia
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Publisher
Elsevier BV
Reference20 articles.
1. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor;Pearce;N Engl J Med,1996
2. Familial hypoparathyroidism: identification of a novel gain of function mutation in transmembrane domain 5 of the calciumsensing receptor;Watanabe;J Clin Endocrinol Metab,1998
3. Moderate hypocalcemia due to normal serum 1,25-dihydroxyvitamin D levels in an asymptomatic kindred with familial hypoparathyroidism;Nolten;Am J Med,1987
4. Mutations in the Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism;Baron;Hum Mol Genet,1996
5. Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation;Pollak;Nat Genet,1994
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