Fragile X Syndrome as an interneuronopathy: a lesson for future studies and treatments
Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability (ID) and a primary genetic cause of autism spectrum disorder (ASD). FXS arises from the silencing of the FMR1 gene causing the lack of translation of its encoded protein, the Fragile X Messenger RibonucleoProtein (...
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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2023-04-01
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| シリーズ: | Frontiers in Neuroscience |
| 主題: | |
| オンライン･アクセス: | https://www.frontiersin.org/articles/10.3389/fnins.2023.1171895/full |
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