MEN1 c.825-1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report-Reference-Cited by-同舟云学术

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MEN1 c.825-1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report

Published:2015-07-29 Issue:4 Volume:12 Page:6152-6156
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

NING ZHIWEI,WANG OU,MENG XUNWU,XING XIAOPING,XIA WEIBO,JIANG YAN,LI MEI,XU YUAN

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 4 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. Unraveling noncoding DNA variants and epimutations: a paradigm shift in hereditary cancer research;Future Oncology;2024-05-09

2. Multiple endocrine neoplasia type 1: a new germline “homozygous” variant (c.201delC) caused by detection errors;Hereditary Cancer in Clinical Practice;2022-03-07

3. Long-term follow-up and novel splice donor mutation in MEN1 in a Chinese family;Oncotarget;2017-12-07

4. Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese;PLOS ONE;2016-11-15

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