机译:PCBD1中的隐性突变导致新型的早期糖尿病
Experimental and Clinical Research Center, Charite Medical Faculty and Max-Delbrueck Center for Molecular Medicine, Berlin, Germany,Cardiovascular and Metabolic Diseases, Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
Laboratory of Molecular and Cellular Basis of Embryonic Development, Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
Experimental and Clinical Research Center, Charite Medical Faculty and Max-Delbrueck Center for Molecular Medicine, Berlin, Germany,Cardiovascular and Metabolic Diseases, Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
Cardiovascular and Metabolic Diseases, Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
Department of Neuroscience, Max-Delbrueck Center for Molecular Medicine,Berlin, Germany;
Division of Genetics, Department of Pediatrics, Nemours Children's Clinic,Jacksonville, FL;
Division of Pediatric Genetics and Metabolism, Department of Pediatrics, University of Minnesota Amplatz Children's Hospital, Minneapolis, MN;
Western Sydney Genetics Program, Royal Alexandra Hospital for Children,Westmead, New South Wales, Australia;
Institute for Experimental Pediatric Endocrinology, Charite Medical Faculty, Berlin, Germany;
Division of Inborn Metabolic Diseases, Department of General Pediatrics, University Children's Hospital, Heidelberg, Germany;
Division of Inborn Metabolic Diseases, Department of General Pediatrics, University Children's Hospital, Heidelberg, Germany,Division of Metabolism, University Children's Hospital, Zuerich, Switzerland;
Laboratory of Molecular and Cellular Basis of Embryonic Development, Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
Cardiovascular and Metabolic Diseases, Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
Experimental and Clinical Research Center, Charite Medical Faculty and Max-Delbrueck Center for Molecular Medicine, Berlin, Germany;
机译:在泰国人中,早发性2型糖尿病的年轻(MODY)基因成熟型糖尿病突变。
机译:在常染色体显性遗传的早发性2型糖尿病家庭中,年轻突变的成熟型糖尿病患病率较高。
机译:没有证据表明法国患有早期II型糖尿病的患者与糖尿病相关的PEK / EIF2AK3基因突变
机译:通过整合突变和表达数据鉴定与2型糖尿病患者的基因签名*
机译:研究与早期发作有关的SCN8A突变的模式。
机译:汉族早期发病的母亲遗传2型糖尿病的HNF4A突变p.T130I和HNF1A突变p.I27L和p.S487N的鉴定
机译:PCBD1的隐性突变导致一种新型的早发型糖尿病