Molecular Biomarkers in Fragile X Syndrome
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability (ID) and a known monogenic cause of autism spectrum disorder (ASD). It is a trinucleotide repeat disorder, in which more than 200 CGG repeats in the 5’ untranslated region (UTR) of the fragile X mental retard...
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| Главные авторы: | , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
MDPI AG
2019-04-01
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| Серии: | Brain Sciences |
| Предметы: | |
| Online-ссылка: | https://www.mdpi.com/2076-3425/9/5/96 |
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