Case Report: Pathogenesis With a Rare RHOA A161E Mutation in a Patient With Angioimmunoblastic T-Cell Lymphoma

Case Report: Pathogenesis With a Rare RHOA A161E Mutation in a Patient With Angioimmunoblastic T-Cell Lymphoma

Angioimmunoblastic T-cell lymphoma (AITL) genomic abnormalities are highly disease-specific, and the ras homology family member A (RHOA) gene is one of the most recurrent mutated genes, especially for RHOA G17V mutation site. Here, we identified a rare RHOA A161E mutation in an AITL patient through...

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Bibliographic Details
Main Authors: Lihong Cao, Hongyan Tong, Xing Liu, Yingqing Xu, Fang Yu, Qi Pan, Jin Lai, Jian Huang, Jiayue Qin, Jie Jin
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Series:Frontiers in Genetics
Subjects:
angioimmunoblastic T-cell lymphoma
hypereosinophilia
RHOA A161E mutation
variant allele frequency
case report
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2022.948744/full

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https://www.frontiersin.org/articles/10.3389/fgene.2022.948744/full

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