LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice-Reference-Cited by-同舟云学术

LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice

Published:2021-05 Issue:5 Volume:48 Page:384-395
ISSN:1673-8527
Container-title:Journal of Genetics and Genomics
language:en
Short-container-title:Journal of Genetics and Genomics

Author:

Yu Li,Wang Lina,Tao Wufan,Zhang Wenxiang,Yang Shuanghao,Wang Jian,Fei Jia,Peng Rui,Wu Yiming,Zhen Xiumei,Shao Hong,Gu Weiyue,Li Rong,Wu Bai-Lin,Wang Hongyan

Funder

Peking University Third Hospital

Fudan University

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology

Reference46 articles.

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3. Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3;Chen;Nat. Genet.,2011

4. Alms1-disrupted mice recapitulate human alström syndrome;Collin;Hum. Mol. Genet.,2005

5. Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in alström syndrome;Collin;Nat. Genet.,2002

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