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...
Сохранить в:
| Главные авторы: | , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Termedia Publishing House
2019-05-01
|
| Серии: | Archives of Medical Science |
| Предметы: | |
| Online-ссылка: | https://www.archivesofmedicalscience.com/The-association-of-FMR1-gene-CGG-n-variation-with-idiopathic-female-infertility,95173,0,2.html |
| Метки: |
Нет меток, Требуется 1-ая метка записи!
|
