Article

Using a Combination of Novel Research Tools to Understand Social Interaction in the<em> Drosophila melanogaster</em> Model for Fragile X Syndrome

2024-04-25

Abstract excerpt

Fragile X syndrome (FXS), the most common monogenic cause of inherited intellectual disability and autism spectrum disorder, is caused by a full mutation (&gt;200 CGG repeats) in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene. Individuals with FXS experience a wide range of challenges related to social interaction (SI). Animal models, such as Drosophila melanogaster model for FXS where the only orthol...

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Literature Corpus work: 28dd0dab-e6c9-5771-9991-ea38818d659a
DOI: 10.20944/preprints202404.1663.v1

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