Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.

scientific article

Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1677/JOE.0.1660001
P698PubMed publication ID10856877
P5875ResearchGate publication ID274443574

P2093author name stringDralle H
Boehm BO
Wagner P
Weitz M
Maier S
Karges W
Wissmann A
Jostarndt K
Feldmann B
Flemming A
P433issue1
P407language of work or nameEnglishQ1860
P921main subjecthyperparathyroidismQ1344835
multiple endocrine neoplasiaQ1553018
primary hyperparathyroidismQ2919083
multiple endocrine neoplasia type 1Q3347154
P304page(s)1-9
P577publication date2000-07-01
P1433published inJournal of EndocrinologyQ6295150
P1476titleMultiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.
P478volume166

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cites work (P2860)
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