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

Name: Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion
Published: 2022-09-25T00:00:00+08:00

NIAID Data Ecosystem2026-03-14 收录

范可尼贫血基因突变

NUP98-HOXC11融合相关白血病

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP397780 数据链接链接失效反馈

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资源简介：

Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion.

创建时间：

2022-09-25

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

资源简介：

相关数据集