A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome-Reference-Cited by-同舟云学术

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A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome

Published:2017-04-12 Issue:6 Volume:15 Page:3735-3738
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Wu Pan-Feng,Jin Jie-Yuan,Li Jing-Jing,He Ji-Qiang,Fan Liang-Liang,Jin Min,Huang Hao,Xia Kun,Tang Ju-Yu,Xiang Rong

Publisher

Spandidos Publications

Subject

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

Cited by 2 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. Severe metabolic disorders coexisting with Werner syndrome: a case report;Endocrine Journal;2021

2. Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency;Trends in Endocrinology & Metabolism;2018-06

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