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
Autores principales: Cao, Lihong, Tong, Hongyan, Liu, Xing, Xu, Yingqing, Yu, Fang, Pan, Qi, Lai, Jin, Huang, Jian, Qin, Jiayue, Jin, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330045/
https://www.ncbi.nlm.nih.gov/pubmed/35910204
http://dx.doi.org/10.3389/fgene.2022.948744

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330045/
https://www.ncbi.nlm.nih.gov/pubmed/35910204
http://dx.doi.org/10.3389/fgene.2022.948744

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