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Charting the future: current and future directions in translational research for individuals with Down syndrome

Abstract The most common genetic cause of intellectual and developmental disability is trisomy of human chromosome 21 (trisomy 21) or Down syndrome. Relative to the general population, individuals with Down syndrome heterogeneously experience atypical morphogenesis, a distinct neurocognitive profile...

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主要な著者: Katherine A. Waugh, Heather M. Wilkins, Keith P. Smith, Lauren T. Ptomey
フォーマット: Artigo
言語:Inglês
出版事項: BMC 2025-07-01
シリーズ:Journal of Neurodevelopmental Disorders
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オンライン・アクセス:https://doi.org/10.1186/s11689-025-09630-8
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