RNA targets of FASTKD2 in Human HEK293 cells
Ontology highlight
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
ACCESS DATA