Congenital thyrotropin deficiency - From discovery to molecular biology, postgenome and preventive medicine

被引:15
作者
Miyai, Kiyoshi [1 ]
机构
[1] Osaka Univ, Osaka, Japan
关键词
TSH deficiency; glycoprotein hormone deficiency; CXGXC motif; central congenital hypothyroidism; neonatal screening;
D O I
10.1507/endocrj.KR-107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:191 / 203
页数:13
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