Whole exome sequencing identifies FBN1 mutations in two patients with early-onset type B aortic dissection-Reference-Cited by-同舟云学术

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Whole exome sequencing identifies FBN1 mutations in two patients with early-onset type B aortic dissection

Published:2017-05 Issue:5 Volume:16 Page:6620-6625
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Han Qian,Zhang Wenwen,Liu Changjian,Zhou Min,Ran Feng,Yi Long,Sun Xitai,Liu Zhao

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. Tracking an Elusive Killer: State of the Art of Molecular-Genetic Knowledge and Laboratory Role in Diagnosis and Risk Stratification of Thoracic Aortic Aneurysm and Dissection;Diagnostics;2022-07-22

2. Rapid identification of a pathogenic variant of PROS1 in a thrombophilic family by whole exome sequencing;Medicine;2021-12-30

3. Sudden death due to a novel nonsense mutation in Marfan syndrome;Legal Medicine;2021-11

4. Postmortem detection of COL gene family variants in two aortic dissection cases;International Journal of Legal Medicine;2021-06-14

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