The 312N variant of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR) confers up to 2·7-fold increased risk of polycystic ovary syndrome in a Sardinian population

Antonio Capalbo, Francesca Sagnella, Rosanna Apa, A. M. Fulghesu, Antonio Lanzone, Andrea Morciano, A. Farcomeni, M. F. Gangale, Francesca Moro, Daniela Martinez, A. Ciardulli, C. Palla, M. L. Uras, F. Spettu, A. Cappai, C. Carcassi, Geraldina Neri, Francesco Danilo Tiziano

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review

33 Citazioni (Scopus)

Abstract

Polycystic ovary syndrome (PCOS) is a frequent condition, affecting about 15% of women of reproductive age. Because of its familial occurrence, a multifactorial model of susceptibility, including both genetic and environmental factors, has been proposed. However, the identification of genetic factors has been elusive.
Lingua originaleEnglish
pagine (da-a)113-119
Numero di pagine7
RivistaClinical Endocrinology
Volume77
DOI
Stato di pubblicazionePubblicato - 2012

Keywords

  • polimorfismi

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