Genomics and AI identify a candidate gene behind rare neurodevelopmental disorder
Researchers at Baylor College of Medicine and the Duncan Neurological Research Institute have identified variants in the BRSK1 gene as a potential cause for a rare neurodevelopmental disorder. The discovery was facilitated by the use of genomics and artificial intelligence.
Why it matters
This finding provides a potential diagnostic path for patients with rare conditions and demonstrates the growing utility of AI in medical research.
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