Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion: A case report

Fanconi anemia (FA) genes play critical roles in the repair of DNA lesions. Non-FA (or underlying FA) patients harboring heterozygous germline FA gene mutations may also face an increased risk of developing bone marrow failure, primary immunodeficiency disease, and hereditary cancer predisposition s...

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Detalles Bibliográficos
Autores principales: Shen, Kefeng, Zhang, Meilan, Wang, Jiachen, Mu, Wei, Wang, Jin, Wang, Chunyan, Xing, Shugang, Hong, Zhenya, Xiao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626966/
https://www.ncbi.nlm.nih.gov/pubmed/36338706
http://dx.doi.org/10.3389/fonc.2022.1036511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626966/
https://www.ncbi.nlm.nih.gov/pubmed/36338706
http://dx.doi.org/10.3389/fonc.2022.1036511

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