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Scoping review highlights shortcomings in social cognition assessment in Duchenne muscular dystrophy, suggesting clinical significance.
dystrophin is highly expressed in structures involved in the brain networks underlying some social cognition skills. Our results, which provide evidence of a gap in the study of social cognition in DMD, underscore the importance of assessing this domain as a possible feature of the CNS phenotype of the disease, consistent with a few other previous reports.
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Parravicini et al. (2026) studied this question.
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