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Focusing on simplex autism, this work investigates the perplexing variation in symptoms among individuals with Autism Spectrum Disorder despite shared genetic backgrounds. By analyzing genetic data alongside phenotypic traits, researchers aim to identify specific gene mutations that correlate with the severity of symptoms. This exploration seeks to unravel the mystery of phenotypic heterogeneity, potentially leading to a better understanding of autism's underlying causes and informing more personalized treatment strategies.
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Unveiling the Mystery of Phenotypic Heterogeneity in Simplex Autism, Sharlin
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- Released
- 2024
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