Unknown,Transcriptomics,Genomics,Proteomics

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RNA targets of FASTKD2 in Human HEK293 cells


ABSTRACT: 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.

ORGANISM(S): Homo sapiens

SUBMITTER: Charles Girardot 

PROVIDER: E-MTAB-4010 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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