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Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.

Abstract:

BACKGROUND: Familial isolated hyperparathyroidism (FIHP) is an autosomal dominant disorder characterized by uniglandular or multiglandular parathyroid tumours that occur in the absence of other endocrine tumours. The disorder may represent either an early stage of multiple endocrine neoplasia type 1 (MEN1), or an allelic variant of MEN1, or a distinct entity involving another locus. We have explored these possibilities in seven families in whom primary hyperparathyroidism occurred as the sole...

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Publication status:
Published

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Journal:
Clinical endocrinology More from this journal
Volume:
58
Issue:
5
Pages:
639-646
Publication date:
2003-05-01
DOI:
EISSN:
1365-2265
ISSN:
0300-0664

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