Clinical recognition and evaluation of patients with inherited serum thyroid hormone-binding protein mutations.

导出 OA

翻译打印收藏纠错

第一作者： M S,Mimoto

第一单位： Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of California, San Diego, 9500 Gilman Drive, MC 7381, San Diego, CA, USA.

作者： M S,Mimoto ^[1] ; S,Refetoff ^[2]

作者单位： Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of California, San Diego, 9500 Gilman Drive, MC 7381, San Diego, CA, USA. ^[1] Department of Medicine, The University of Chicago MC3090, 5841 South Maryland Avenue, Chicago, IL, 60637, USA. srefetof@uchicago.edu.;Department of Pediatrics, The University of Chicago MC3090, 5841 South Maryland Avenue, Chicago, IL, 60637, USA. srefetof@uchicago.edu.;Committee on Genetics, The University of Chicago MC3090, 5841 South Maryland Avenue, Chicago, IL, 60637, USA. srefetof@uchicago.edu. ^[2]

关键词 Familial dysalbuminemic hyperthyroxinemia Human serum albumin Serum thyroid hormone-binding proteins TBG deficiency Thyroxine-binding globulin Transthyretin

主题词载体蛋白质类(Carrier Proteins);评价研究(主题)(Evaluation Studies as Topic);人类(Humans);膜蛋白质类(Membrane Proteins);突变(Mutation);甲状腺疾病(Thyroid Diseases);甲状腺激素类(Thyroid Hormones)

DOI 10.1007/s40618-019-01084-9

PMID 31352644

发布时间 2023-12-13

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交