The most common disease-causing mutation of factor XIII deficiency is corrected by CRISPR/CAS9 gene editing system-Reference-Cited by-同舟云学术

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The most common disease-causing mutation of factor XIII deficiency is corrected by CRISPR/CAS9 gene editing system

Published:2022-02-25 Issue:3 Volume:33 Page:153-158
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Dorgalaleh Akbar,Kiani Jafar,Zaker Farhad,Safa Majid

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference17 articles.

1. Blood coagulation factor XIII and factor XIII deficiency;Dorgalaleh;Blood Rev,2016

2. Diagnosis and classification of factor XIII deficiencies;Kohler;J Thromb Haemost,2011

3. Successful correction of factor V deficiency of patient-derived iPSCs by CRISPR/Cas9-mediated gene editing;Nakamura;Haemophilia,2020

4. CRISPR/Cas9-mediated somatic correction of a novel coagulator factor IX gene mutation ameliorates hemophilia in mouse;Guan;EMBO Mol Med,2016

5. CRISPR/Cas9- mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice;Huai;Hum Genet,2017

Cited by 1 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. The History of Factor XIII Deficiency;Seminars in Thrombosis and Hemostasis;2023-01-27

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