Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development-Reference-Cited by-同舟云学术

Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development

Published:2018-06-15 Issue:7 Volume:33 Page:1364-1369
ISSN:0268-1161
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Chen C¹,Xu X²,Kong L²,Li P²,Zhou F²,Zhao S²,Xin X²,Tan J²,Zhang X¹³

Affiliation:

1. The Research Center for Medical Genomics, Key Laboratory of Cell Biology, Ministry of Public Health, Key Laboratory of Medical Cell Biology, Ministry of Education, College of Basic Medical Science, China Medical University, No. 77 Puhe Road, North New Area, Shenyang, China

2. Reproductive Medical Center of Gynecology and Obstetrics, Shengjing Hospital Affiliated to China Medical University, No. 39 Huaxiang Road, Tiexi, Shenyang, China

3. McKusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, No. 5 Dongdan Santiao, Beijing, China

Funder

National High-tech R&D Program of China

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynaecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/33/7/1364/25071092/dey215.pdf

Reference18 articles.

1. Empty follicle syndrome prevalence and management in oocyte donors;Blazquez;Hum Reprod,2014

2. A recurrent missense mutation in ZP3 causes empty follicle syndrome and female infertility;Chen;Am J Hum Genet,2017