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机译:与低钾性周期性麻痹相关的CACNA1S基因的新型突变,其穿透性存在性别差异
Genomics Research Center, Harbin Medical University, Harbin, China;
Neurology Department of The First Affiliated Hospital, Harbin Medical University, Harbin, China;
Genomics Research Center, Harbin Medical University, Harbin, China;
Genomics Research Center, Harbin Medical University, Harbin, China;
Genomics Research Center, Harbin Medical University, Harbin, China;
Genomics Research Center, Harbin Medical University, Harbin, China;
Neurology Department of The First Affiliated Hospital, Harbin Medical University, Harbin, China;
Genetic Detection Center, Harbin Medical University, Harbin, China;
Neurology Department of The First Affiliated Hospital, Harbin Medical University, Harbin, China;
Genomics Research Center, Harbin Medical University, Harbin, China;
Hypokalemic periodic paralysis; Gene mapping; Mutation; CACNA1S; Gender difference; Penetrance;
机译:与低钾性周期性麻痹相关的CACNA1S基因的新型突变,其穿透性存在性别差异
机译:伴有CACNA1S基因突变的低钾性周期性麻痹症患者的外露能力不完全。
机译:低钾性周期性麻痹的外表力和表型性别差异
机译:血液周期异常中人肌肉膜行为的理论分析
机译:新型向内整流钾通道(Kir2.6)的表征及其在甲状腺毒性低钾性周期性麻痹中的作用。
机译:CaCNA1s基因突变引起的低钾血糖定期瘫痪
机译:用CaCNA1S基因突变进行低钾血糖瘫痪,显示女性不完全渗透