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Molecular genetics in familial primary hyperparathyroidism: A study from Northern India

2024-11-04

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<title>Abstract</title> <p>Purpose Familial primary hyperparathyroidism (FPHPT) accounts for about 10% of cases, owing to germline mutations in specific genes. The genetic profile of FPHPT has not been studied in our population. This is most likely the first study in our region to examine the genetic profile to search for any other PHPT-related tumours in these patients. Methods This prospective cross-sectional...

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Literature Corpus work: b71163e3-a70d-55c2-8d20-84258543f5cb
DOI: 10.21203/rs.3.rs-5299691/v1

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