A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding

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A variant in the 3′ UTR of human SCN1A gene from Dravet patient decreases mRNA stability mediated by GAPDH http://t.co/K2jgL84kSH Hum Gen

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A variant in the 3′ UTR of human SCN1A gene from Dravet patient decreases mRNA stability mediated by GAPDH http://t.co/K2jgL84kSH Hum Gen

Reply Repost Favourite