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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Detalles Bibliográficos

Principais autores:	Lihong Cao, Hongyan Tong, Xing Liu, Yingqing Xu, Fang Yu, Qi Pan, Jin Lai, Jian Huang, Jiayue Qin, Jie Jin
Formato:	Artigo
Idioma:	Inglês
Publicado:	Frontiers Media S.A. 2022-07-01
Series:	Frontiers in Genetics
Assuntos:	angioimmunoblastic T-cell lymphoma hypereosinophilia RHOA A161E mutation variant allele frequency case report
Acceso en liña:	https://www.frontiersin.org/articles/10.3389/fgene.2022.948744/full
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