RNA targets of FASTKD2 in Human HEK293 cells
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https://www.ncbi.nlm.nih.gov/sra/ERP012948
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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



