A new study has found that rapid genome sequencing is a fast and effective way to diagnose infant epilepsy, a condition that, if left untreated, can lead to developmental delays. The researchers hope that their findings mean this cutting-edge technology will become more widely available.Continue ReadingCategory: Medical, ScienceTags: Epilepsy, Children, Genome, Murdoch Childrens Research Institut
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Rapid genome sequencing could revolutionize infant epilepsy diagnosis
Posted by ArielTechGeek 621 days ago (https://newatlas.com)
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