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
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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发表时间：
2014
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作者：
Long YS;Dong ZF;Liu SJ;Wan RP;Tang LJ;Liu T;Zhao QH;Shi YW;Yi YH;
