机译:新的等位基因变异和尿布突变的证据,导致肾低度血症:生物化学,遗传学和功能分析
Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in Prague;
Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in Prague;
Department of Pathophysiology Tokyo University of Pharmacy and Life Sciences Tokyo Japan;
Department of Pathophysiology Tokyo University of Pharmacy and Life Sciences Tokyo Japan;
Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in Prague;
Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in Prague;
Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in Prague;
Institute of Inherited Metabolic Disorders First Faculty of Medicine Charles University in Prague;
renal hypouricemia; SLC22A12; URAT1; uric acid transporters;
机译:新型等位基因变体和导致肾脏低尿酸血症的URAT1普遍突变的证据:生化,遗传和功能分析
机译:URAT1和GLUT9中新的等位基因变异导致1型和2型肾低尿酸血症的功能分析
机译:URAT1和Glut9新型等位基因变体的功能分析,导致肾小血症1和2
机译:在多个等位基因变体对比较氢交换质谱分析中处理序列变异性
机译:骨形态发生蛋白9的结构和功能分析:骨形态发生蛋白9的晶体结构,与前域和受体的结合研究以及果蝇十足性果蝇的突变研究
机译:新型等位基因变体和导致肾性低尿酸血症的URAT1普遍突变的证据:生化遗传和功能分析
机译:新的等位基因变异和尿布突变的证据,导致肾脏低血肿:生化,遗传学和功能分析