Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism.
Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism.
复制标题
促甲状腺素受体基因的组成性活跃种系突变是先天性甲状腺功能亢进症的原因。
作者：
K. Schwab,;M. Gerlich;M. Broecker;P. Söhlemann;M. Derwahl;M. Lohse
影响因子：
6.6
作者：
MCKENZIE, JM;ZAKARIJA, M
通讯作者：
ZAKARIJA, M