Scientists have demonstrated that variants in the SPTBN1 gene can alter neuronal architecture, dramatically affecting their function and leading to a rare, newly defined neurodevelopmental syndrome in children.
from Latest Science News -- ScienceDaily https://www.sciencedaily.com/releases/2021/07/210701112644.htm
from Latest Science News -- ScienceDaily https://www.sciencedaily.com/releases/2021/07/210701112644.htm
Scientists find genetic cause, underlying mechanisms of new neurodevelopmental syndrome
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July 02, 2021
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