Identification of 3'-UTR single nucleotide variants and prediction of select protein imbalance in mesial temporal lobe epilepsy patients.

PLoS One · 2021 · PMC8177469 · PMID 34086756

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may be significantno p-value reported

Similarly, our finding of 3’-UTR SNVs in HERC2 ( Table 2 ) may be significant because altered expression of HERC1 , which belongs to the same family as HERC2 , is shown to be associated with FS [ 63 ].

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