Researchers discovered the cause of a rare genetic condition causing seizures and delayed development, focusing on glutamine's role in brain development.
Researchers at the University of Otago, along with international collaborators, discovered the cause of a rare genetic condition that leads to seizures and delayed development. The study, published in The American Journal of Human Genetics, focused on glutamine's role in brain development. Identifying this genetic disorder's cause may pave the way for recognition, diagnosis, and treatments for such rare conditions.
April 15, 2024
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