Hypergonadotropic hypogonadism and renal failure due to WT1 mutation

被引：3

作者：

Benz, Kerstin

Plank, Christian

Amann, Kerstin

Mucha, Bettina

Doerr, Helmuth G.

Rascher, Wolfgang

Doetsch, Jorg

机构：

[1] Univ Erlangen Nurnberg, Klin Kinder & Jugendliche, D-91054 Erlangen, Germany

[2] Univ Erlangen Nurnberg, Dept Pathol, Erlangen, Germany

[3] Dept Pediat & Human Genet, Ann Arbor, MI USA

来源：

NEPHROLOGY DIALYSIS TRANSPLANTATION | 2006年 / 21卷 / 06期

关键词：

focal segmental glomerulonephritis; Frasier syndrome; germ cell neoplasia; hypergonadotropic hypogonadism; pubertal development; Wilms' tumour 1 mutation;

D O I：

10.1093/ndt/gfl023

中图分类号：

R3 [基础医学]; R4 [临床医学];

学科分类号：

1001 ; 1002 ; 100602 ;

摘要：

[No abstract available]

引用

页码：1716 / 1718

页数：3

共 16 条

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