Role of the mutations Trp8 ⇒ Arg and Ile15 ⇒ Thr of the human luteinizing hormone β-subunit in women with polycystic ovary syndrome
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference23 articles.
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3. Identification of two point mutations in the gene coding luteinizing hormone (LH) β-subunit, associated with immunologically anomalous LH variants;Furui;J Clin Endocrinol Metab,1994
4. Occurrence and biological properties of a common genetic variant of luteinizing hormone;Haavisto;J Clin Endocrinol Metab,1995
5. Worldwide frequency of a common genetic variant of luteinizing hormone;Fertil Steril,1997
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1. Association of Luteinizing hormone and LH receptor gene polymorphism with susceptibility of Polycystic ovary syndrome;Systems Biology in Reproductive Medicine;2019-04-08
2. Two Hormones for One Receptor: Evolution, Biochemistry, Actions, and Pathophysiology of LH and hCG;Endocrine Reviews;2018-06-13
3. LH (Trp8Arg/Ile15Thr), LHR (insLQ) and FSHR (Asn680Ser) polymorphisms genotypic prevalence in women with endometriosis and infertility;Journal of Assisted Reproduction and Genetics;2015-05-03
4. ‘Carriers of V‐LH among 1593 Baltic men have significantly higher serum LH’;Andrology;2015-03-26
5. Trp28Arg/Ile35Thr LHB gene variants are associated with elevated testosterone levels in women with polycystic ovary syndrome;Gene;2014-10
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