Congenital hypothyroidism caused by a mutation in the Na+/I- symporter

被引：106

作者：

Fujiwara, H

Tatsumi, K

Miki, K

Harada, T

Miyai, K

Takai, S

Amino, N

机构：

[1] KOSHIEN UNIV, COLL NUTR, DEPT LAB MED, TAKARAZUKA, HYOGO 665, JAPAN

[2] KOSHIEN UNIV, COLL NUTR, DEPT PEDIAT, TAKARAZUKA, HYOGO 665, JAPAN

[3] OSAKA UNIV, SCH MED, DEPT SURG ONCOL, OSAKA 565, JAPAN

来源：

NATURE GENETICS | 1997年 / 16卷 / 02期

关键词：

D O I：

10.1038/ng0697-124

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：124 / 125

页数：2

共 12 条

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[9] CRETINISM WITH COMBINED HORMONE DEFICIENCY CAUSED BY A MUTATION IN THE PIT1 GENE
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[J]. NATURE GENETICS, 1992, 1 (01) : 56 - 58
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