Conference item
Genetics of parathyroid tumours
- Abstract:
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Primary hyperparathyroidism (PHPT), due to parathyroid tumours, may occur as part of a complex syndrome or as an isolated (non-syndromic) disorder, and both forms can occur as familial (i.e. hereditary) or non-familial (i.e. sporadic) disease. Syndromic PHPT includes multiple endocrine neoplasia (MEN) types 1 to 4 (MEN1 to MEN4) and the hyperparathyroidism-jaw tumour (HPT-JT) syndrome. Syndromic and hereditary PHPT are often associated with multiple parathyroid tumours, in contrast to spora...
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- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Accepted manuscript, pdf, 489.8KB)
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- Publisher copy:
- 10.1111/joim.12523
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Authors
Funding
+ National Institute for Health Research
More from this funder
Funding agency for:
Thakker, R
Grant:
G10001167
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Bibliographic Details
- Publisher:
- Wiley Publisher's website
- Journal:
- Journal of Internal Medicine Journal website
- Volume:
- 280
- Issue:
- 6
- Pages:
- 574–583
- Host title:
- Journal of Internal Medicine
- Publication date:
- 2016-06-01
- Acceptance date:
- 2017-05-12
- DOI:
- Source identifiers:
-
622984
Item Description
- Keywords:
- Pubs id:
-
pubs:622984
- UUID:
-
uuid:bdddf37b-2830-4771-931f-3ab9175d5875
- Local pid:
- pubs:622984
- Deposit date:
- 2016-05-19
Terms of use
- Copyright holder:
- Association for the Publication of the Journal of Internal Medicine
- Copyright date:
- 2016
- Notes:
- © 2016 The Association for the Publication of the Journal of Internal Medicine. This is the accepted manuscript version of the article. The final version is available online from Wiley at: [10.1111/joim.12523]
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