Whole-exome sequencing identified the mutation of IRF5 in thymic Rosai-Dorfman disease: A case report-Reference-Cited by-同舟云学术

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Whole-exome sequencing identified the mutation of IRF5 in thymic Rosai-Dorfman disease: A case report

Published:2023-11 Issue:11 Volume:46 Page:5055-5057
ISSN:1015-9584
Container-title:Asian Journal of Surgery
language:en
Short-container-title:Asian Journal of Surgery

Author:

Lv Changsheng^ORCID,Zhong Lin,Wang Zhaoxuan,Zhao Lei

Publisher

Elsevier BV

Subject

Surgery

Reference4 articles.

1. Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease;Abla;Blood,2018

2. Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease;Morgan;PLoS Genet,2010

3. Advances and challenges in targeting IRF5, a key regulator of inflammation;Almuttaqi;FEBS J,2019

4. Association of IRF5 polymorphisms with susceptibility to hemophagocytic lymphohistiocytosis in children;Yanagimachi;J Clin Immunol,2011

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