No Evidence of Germline Mutation or Somatic Deletion of the MEN1 Gene in a Case of Familial Multiple Endocrine Neoplasia Type 1(MEN1).-Reference-Cited by-同舟云学术

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No Evidence of Germline Mutation or Somatic Deletion of the MEN1 Gene in a Case of Familial Multiple Endocrine Neoplasia Type 1(MEN1).

Published:1999 Issue:6 Volume:46 Page:811-816
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

NAMIHIRA HIROYOSHI¹,SATO MAKOTO¹,MATSUBARA SHUJI¹,OHYE HIDEMI¹,BHUIYAN MMR¹,MURAO KOJI¹,TAKAHARA JIRO¹

Affiliation:

1. First Department of Internal Medicine, Kagawa Medical University

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj1993/46/6/46_6_811/_pdf

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel germline variants of CDKN1B and CDKN2C identified during screening for familial primary hyperparathyroidism;Journal of Endocrinological Investigation;2022-11-05

2. Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features;PLOS ONE;2017-10-16

3. MEN4 and CDKN1B mutations: the latest of the MEN syndromes;Endocrine-Related Cancer;2017-10

4. Molecular Pathogenesis of Primary Hyperparathyroidism;Handbook of Parathyroid Diseases;2011-12-28

5. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans;Proceedings of the National Academy of Sciences;2006-10-09

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