Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure

被引：91

作者：

Watkins, Wendy J.

Umbers, Alexandra J.

Woad, Kathryn J.

Harris, Sarah E.

Winship, Ingrid M.

Gersak, Ksenija

Shelling, Andrew N.

机构：

[1] Univ Auckland, Dept Obstet & Gynaecol, Fac Med & Hlth Sci, Auckland 1, New Zealand

[2] Prince Henrys Inst Med Res, Clayton, Vic, Australia

[3] Univ Edinburgh, Dept Psychol, Edinburgh EH8 9YL, Midlothian, Scotland

[4] Royal Childrens Hosp, Genet Hlth Serv, Parkville, Vic 3052, Australia

[5] Univ Ljubljana, Med Ctr, Dept Obstet & Gynaecol, Ljubljana 61000, Slovenia

来源：

FERTILITY AND STERILITY | 2006年 / 86卷 / 05期

关键词：

D O I：

10.1016/j.fertnstert.2006.03.054

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

FOXO3A and FOXO1A are excellent candidate genes for the development of premature ovarian failure and have not been analyzed previously in POF patients. Potentially causal mutations in FOX03A (2/90; 2.2%) and FOXO1A (1 /90; 1.1%) were identified in POF patients; however, the pathological role of these mutations will be determined only by screening increased numbers of patients and controls, or by functional studies. (Fertil Steril (R) 2006;86:1518-21. (c) 2006 by American Society for Reproductive Medicine.)

引用

页码：1518 / 1521

页数：4

共 16 条

[11] Identification of novel mutations in FOXL2 associated with premature ovarian failure [J].