How polymorphic markers contribute to genetic diseases in different populations? The study of inhibin A for premature ovarian insufficiency

OBJECTIVE: To verify the incidence of the G679A mutation in exon 2 of the gene inhibin alpha (INHA), in women with secondary amenorrhea and diagnosis of premature ovarian insufficiency, and in controls. METHODS: A 5mL sample of peripheral blood was collected from all study participants in an EDTA tu...

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Dettagli Bibliografici
Pubblicato in:Einstein (Sao Paulo)
Autori principali: Christofolini, Denise Maria, Cordts, Emerson Barchi, Santos-Pinheiro, Fernando, Kayaki, Erika Azuma, Dornas, Mayla Cristina Fernandes, Santos, Monise de Castro, Bianco, Bianca, Barbosa, Caio Parente
Natura: Artigo
Lingua:Inglês
Pubblicazione: Instituto Israelita de Ensino e Pesquisa Albert Einstein 2017
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Original Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5823038/
https://ncbi.nlm.nih.gov/pubmed/29091146
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1679-45082017AO4052
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