Pure haploinsufficiency for Dravet syndrome NaV1.1 (SCN1A) sodium channel truncating mutations: No Negative Dominance for Dravet Syndrome Truncated NaV1.1 MutantsGiulia Bechi,Paolo Scalmani,Emanuele Schiavon,Raffaella Rusconi,Silvana Franceschetti,Massimo MantegazzaEpilepsia(2012)引用 23|浏览9暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要