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机译:患有持续性超胰岛素血症低血糖,心脏缺陷和严重的肺胰剂的患者中的CACNA1D CACNA1D CACNA1D突变
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Medical Genetics ServiceHospital de Clínicas de Porto AlegrePorto Alegre RS Brazil;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
Developmental Endocrinology Research Group Clinical and Molecular Genetics UnitUCL Institute of;
Institute of Biomedical and Clinical ScienceUniversity of Exeter Medical SchoolExeter UK;
CACNA1D; calcium channel; exome sequencing; hyperinsulinism; hypoglycaemia;
机译:患有持续性超胰岛素血症低血糖,心脏缺陷和严重的肺胰剂的患者中的CACNA1D CACNA1D CACNA1D突变
机译:含CaCNA1D CaCNA1D基因缺失的1型半织物状干细胞表现出降低增殖和下降的神经元命运选择
机译:CaCNA1D de Novo突变的生物物理分类为严重神经发育障碍的高危突变
机译:使用头戴式显示器(HMD)系统评估视野缺损患者的视觉空间识别:严重视野缺损的案例研究
机译:严重肺动脉高压患者丛状病变内基因表达的突变和表观遗传调控。
机译:持续性高胰岛素血症性低血糖心脏缺陷和严重低渗症患者的CACNA1D突变
机译:患有持续性高胰岛素血症性低血糖,心脏缺陷和严重低渗的患者的CACNA1D突变。