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Journal article

Molecular genetics of parathyroid disease

Abstract:

Recent advances in molecular biology and cytogenetics have made it possible to localize, clone, and characterize some of the genetic abnormalities that result in parathyroid diseases. Thus mutations in the recently cloned calcium-sensing receptor gene have been reported in patients with familial benign hypercalcemia and autosomal dominant hypocalcemia, and the role of PRAD1 has revealed a novel cyclin to be involved in the pathogenesis of some parathyroid tumors. In addition, muta-tions in th...

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Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
OCDEM
Role:
Author
Journal:
Current Opinion in Endocrinology and Diabetes
Volume:
3
Issue:
6
Pages:
521-528
Publication date:
1996-01-01
DOI:
ISSN:
1068-3097
Source identifiers:
94205
Language:
English
Pubs id:
pubs:94205
UUID:
uuid:3e98fd99-6ff5-486c-85fc-0095c6375d0b
Local pid:
pubs:94205
Deposit date:
2012-12-19

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