RNA targets of FASTKD2 in Human HEK293 cells
收藏NIAID Data Ecosystem2026-05-01 收录
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资源简介：
A mutation within FASTKD2 causes a rare form of Mendelian mitochondrial encephalomyopathy. To investigate whether and how RNA binding of FASTKD2 contributes to the disease phenotype, we identified the RNA targets of FASTKD2 by iCLIP.
创建时间：
2023-10-13
