A mutant single nucleotide polymorphism of follicle-stimulating hormone receptor is associated with a lower risk of endometriosis

Six hundred thirty-seven Taiwanese Chinese women including 300 patients with endometriosis and 337 controls without endometriosis were enrolled to investigate the association between nonsynonymous single nucleotide polymorphism of the FSH receptor gene and the risk of endometriosis. For the A/G poly...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Fertility and sterility 2011, Vol.95 (1), p.455-457
Hauptverfasser:	Wang, Hsin-Shih, M.D., Ph.D, Cheng, Bi-Hwa, M.D, Wu, Hsien-Ming, M.D., Ph.D, Yen, Chih-Feng, M.D, Liu, Chun-Ting, M.Sc, Chao, Angel, M.D., Ph.D, Wang, Tzu-Hao, M.D., Ph.D
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Asian Continental Ancestry Group - genetics Asian Continental Ancestry Group - statistics & numerical data Biological and medical sciences Endometriosis Endometriosis - epidemiology Endometriosis - genetics Female Female genital diseases follicle-stimulating hormone follicle-stimulating hormone receptors genes Genetic Predisposition to Disease - epidemiology Genotype Gynecology. Andrology. Obstetrics Humans Internal Medicine matrix-assisted laser desorption-ionization time-of-flight mass spectrometry (MALDI-TOF MS) Medical sciences Middle Aged mutants Non tumoral diseases Obstetrics and Gynecology patients Polymorphism, Single Nucleotide Receptors, FSH - genetics risk Risk Factors single nucleotide polymorphism single nucleotide polymorphism (SNP) Taiwan - epidemiology women
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!