Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference156 articles.
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4. 1998. Marked hypercalcemia in a five-month-old male associated with heterozygous point mutation in the calcium-sensing receptor gene. Prog & Abs 80th Ann Meet Endo Abs P3-535. p 495.
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