A mutant single nucleotide polymorphism of follicle-stimulating hormone receptor is associated with a lower risk of endometriosis
This study investigated a specific single nucleotide polymorphism in the follicle-stimulating hormone receptor and found it associated with a reduced risk of developing endometriosis.
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References (14)
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Cited by (9)
- Epidemiologic factors associated with endometriosis in East Asia 2019
- A review of the risk factors, genetics and treatment of endometriosis in Chinese women: a comparative update 2018
- Associations between a single nucleotide polymorphism of stress-induced phosphoprotein 1 and endometriosis/adenomyosis 2018
- The Impact of <i>FSHR</i> Gene Polymorphisms Ala307Thr and Asn680Ser in the Endometriosis Development 2018
- LH (Trp8Arg/Ile15Thr), LHR (insLQ) and FSHR (Asn680Ser) polymorphisms genotypic prevalence in women with endometriosis and infertility 2015
- Understanding the role of epigenomic, genomic and genetic alterations in the development of endometriosis (Review) 2014
- Follicle-stimulating hormone receptor gene polymorphisms in women with endometriosis 2014
- TP53 gene polymorphisms at codons 11, 72, and 248 and association with endometriosis in a Brazilian population 2014
- Functional Analyses of Endometriosis-Related Polymorphisms in the Estrogen Synthesis and Metabolism-Related Genes 2012
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- europepmc
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