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Problems in synapse connection sites found in rare neurodevelopmental disorders
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Problems in synapse connection sites found in rare neurodevelopmental disorders

Researchers at Karolinska Institutet describe molecular and cellular consequences of unique genetic mutations affecting the CASK gene which has been implicated in various neurodevelopmental disorders. Notably, the results indicate differences in the development of presynapses of inhibitory neurons in individuals with specific mutations. The findings elucidate key mechanisms during early neuronal maturation and may help...