机译:叶酸转运蛋白基因的突变和人骨髓细胞的风险
Division of NeonatologyThe University of Texas Health Science Center at HoustonHouston Texas;
Division of NeonatologyThe University of Texas Health Science Center at HoustonHouston Texas;
Division of Medical Genetics Department of Pediatrics McGovern Medical SchoolThe University of;
Department of Epidemiology Human Genetics and Environmental Sciences School of Public HealthThe;
Department of Epidemiology Human Genetics and Environmental Sciences School of Public HealthThe;
Division of Medical Genetics Department of Pediatrics McGovern Medical SchoolThe University of;
Division of Medical Genetics Department of Pediatrics McGovern Medical SchoolThe University of;
folate receptors; folate transporters; myelomeningocele (MM); neural tube defects (NTDs);
机译:叶酸转运蛋白基因的突变和人骨髓细胞的风险
机译:叶酸转运蛋白突变和骨髓细胞瘤
机译:鉴别葡萄糖稳态/氧化应激和叶酸/单碳代谢网络中骨髓细胞的新候选风险基因
机译:人肝的钠型胆汁盐吸收转运蛋白中的突变,SLC21A6
机译:人类遗传疾病的多种机制:COL1A2基因的剪接顺序确定。影响成骨不全症中剪接位点突变和易位破坏SNRPN基因的效应会导致Prader-Willi综合征。
机译:叶酸转运蛋白基因的突变和人类髓鞘膜膨大的风险。
机译:叶酸转运蛋白基因的突变和人骨髓细胞的风险
机译:诱导小鼠突变和人类遗传风险评估