机译:IL12RB1基因新型双等异位突变的患者的传染病,自身免疫和中线缺陷
Baskent Univ Fac Med Dept Pediat Div Pediat Allergy &
Immunol Ankara Turkey;
Necmettin Erbakan Univ Meram Fac Med Dept Pediat Div Pediat Allergy &
Immunol Konya Turkey;
Necmettin Erbakan Univ Meram Fac Med Div Pediat Hematol Konya Turkey;
INSERM Lab Human Genet Infect Dis Necker Branch U1163 F-75654 Paris 13 France;
INSERM Lab Human Genet Infect Dis Necker Branch U1163 F-75654 Paris 13 France;
Antalya Technopark Babylife Cord Blood Bank &
St Dept Pediat Div Pediat Allergy &
Immunol;
Antalya Technopark Babylife Cord Blood Bank &
St Antalya Turkey;
INSERM Lab Human Genet Infect Dis Necker Branch U1163 F-75654 Paris 13 France;
INSERM Lab Human Genet Infect Dis Necker Branch U1163 F-75654 Paris 13 France;
INSERM Lab Human Genet Infect Dis Necker Branch U1163 F-75654 Paris 13 France;
INSERM Lab Human Genet Infect Dis Necker Branch U1163 F-75654 Paris 13 France;
autoimmunity; IL-12R beta 1 deficiency; midline defect; salmonellosis;
机译:IL12RB1基因新双等位基因突变患者的传染病,自身免疫和中线缺陷
机译:在分化中具有选择性缺陷的患者中IL12RB1的杂合酶突变
机译:脑内UGP2的丧失导致严重的癫痫发作性,强调基本基因的双位等异构类特异性起始损失可导致遗传疾病
机译:自身免疫,传染病和肿瘤的T调节细胞
机译:PolySearch:一种基于Web的文本挖掘系统,用于提取人类疾病,基因,突变,药物和代谢物之间的关系
机译:孟德尔易感分枝杆菌病的中国患者中的三个新的复合杂合子IL12RB1突变
机译:脑内UGP2的丧失导致严重的癫痫脑病,强调生物等异构体的必要基因的特异性起始损失突变会导致遗传疾病