机译:双腿人瘙痒痒变体导致多系统疾病具有疑似特征:第二次报告
Department of Clinical Genetics North East Thames Regional Genetics ServiceGreat Ormond Street;
Department of Occupational &
Environmental MedicineRoyal Brompton &
Harefield NHS Foundation;
Department of Paediatric Respiratory MedicineRoyal Brompton &
Harefield NHS Foundation TrustLondon;
Department of EndocrinologyGreat Ormond Street Hospital for Children NHS Foundation Trust &
Department of Clinical Genetics North East Thames Regional Genetics ServiceGreat Ormond Street;
asthma; camptodactyly; chronic lung disease; dysmorphism; ITCH; short stature;
机译:双腿人瘙痒痒变体导致多系统疾病具有疑似特征:第二次报告
机译:瘙痒基因的突变会导致综合征多系统自身免疫疾病与急性肝衰竭
机译:PROMIS ITCH调查问卷的发展,验证和解释:患者对瘙痒的生命影响质量的患者
机译:报告人类疾病的爆发
机译:小鼠和人类感觉神经元急性和慢性瘙痒的分子介导物
机译:人类ITCH E3泛素连接酶缺乏症导致多系统综合征的自身免疫性疾病
机译:人类ITCH E3泛素连接酶缺乏症导致多系统综合征的自身免疫性疾病