Neurogenetics and Gene Therapies Across the Motor Axis
Advancements in CRISPR, antisense oligonucleotides, and whole-exome sequencing (WES) are transforming treatment strategies for disorders like SMA, ALS, and hereditary neuropathies. This session bridges central and peripheral pathologies, focusing on translational breakthroughs from bench to bedside.Delegates gain insights into regulatory approvals and clinical pipelines. Young researchers can engage with top genomic labs, while poster presenters can showcase rare mutation studies. Students will benefit from interactive tutorials on sequencing platforms and variant interpretation.
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