Early Onset Primary Hyperparathyroidism Associated with a Novel Germline Mutation in CDKN1B
Individuals presenting with primary hyperparathyroidism (PHPT) at a young age commonly have an underlying germline gene mutation in one of the following genes: MEN1, CASR, or CDC73. A small number of families with primary hyperparathyroidism have been identified with germline mutations in CDKN1B and...
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Main Authors: | Marianne S. Elston, Goswin Y. Meyer-Rochow, Michael Dray, Michael Swarbrick, John V. Conaglen |
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Format: | Article |
Language: | English |
Published: |
Wiley
2015-01-01
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Series: | Case Reports in Endocrinology |
Online Access: | http://dx.doi.org/10.1155/2015/510985 |
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