Скачать или смотреть ADHD Gene Discovery: Rare Mutations in MAP1A, ANO8, and ANK2

Uncover the groundbreaking research that sheds light on the genetic basis of ADHD. Scientists have identified rare mutations in three genes, MAP1A, ANO8, and ANK2, which significantly increase the risk of developing ADHD. This video explores how these mutations disrupt neuron communication and impact brain development, offering new insights into the disorder's biological mechanisms.
Learn about the large-scale genetic analysis conducted by an international team, their findings on the role of these genes in fetal brain development, and the potential implications for future treatments. Discover how these rare variants contribute to the diagnosis and affect life outcomes, including educational attainment and socioeconomic status.
Explore the cellular and molecular mechanisms behind ADHD and the potential for more targeted pharmaceutical interventions. Stay tuned for an in-depth look at this fascinating study and its implications for ADHD research and treatment.