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Congenital thyrotropin deficiency - From discovery to molecular biology, postgenome and preventive medicine
被引:15
作者
:
Miyai, Kiyoshi
论文数:
0
引用数:
0
h-index:
0
机构:
Osaka Univ, Osaka, Japan
Osaka Univ, Osaka, Japan
Miyai, Kiyoshi
[
1
]
机构
:
[1]
Osaka Univ, Osaka, Japan
来源
:
ENDOCRINE JOURNAL
|
2007年
/ 54卷
/ 02期
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
相关论文
共 82 条
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→
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SITE-SPECIFIC MUTAGENESIS OF HUMAN CHORIONIC-GONADOTROPIN (HCG)-BETA SUBUNIT - INFLUENCE OF MUTATION ON HCG PRODUCTION
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