Congenital hypothyroidism and thyroid dyshormonogenesis: a case report of siblings with a newly identified mutation in thyroperoxidase
先天性甲状腺功能减退症和甲状腺激素合成障碍:一对兄妹携带新发现的甲状腺过氧化物酶基因突变的病例报告
期刊:Journal of Pediatric Endocrinology & Metabolism
影响因子:1
doi:10.1515/jpem-2015-0253
Sparling, David P; Fabian, Kendra; Harik, Lara; Jobanputra, Vaidehi; Anyane-Yeboa, Kwame; Oberfield, Sharon E; Fennoy, Ilene