Unusual SMN1 mutations detected with ultra-long DNA sequencing
Study highlight’s role of ultra-LRS in treating the condition clinically Two young patients with spinal muscular atrophy (SMA) were found to have rare mutations in their SMN1 gene, according to a study that employed ultra-long read sequencing (ultra-LRS) to analyze extensive DNA segments. The research, published in Neuromuscular Disorders, emphasizes the significance of ultra-LRS in … Read more