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The association of FMR1 gene (CGG)n variation with idiopathic female infertility

Introduction The FMR1 gene plays an important role in brain development and in the regulation of ovarian function. The FMR1 gene contains CGG repeat variation and the expansion of the repeats is associated with various phenotypes e.g. fragile X syndrome, premature ovarian failure, etc. Repeats rangi...

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Главные авторы: Adele Grasmane, Dmitrijs Rots, Zane Vitina, Valerija Magomedova, Linda Gailite
Формат: Artigo
Язык:Inglês
Опубликовано: Termedia Publishing House 2019-05-01
Серии:Archives of Medical Science
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Online-ссылка:https://www.archivesofmedicalscience.com/The-association-of-FMR1-gene-CGG-n-variation-with-idiopathic-female-infertility,95173,0,2.html
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