Studying mitochondrial disorders, which result from mitochondrial dysfunction, can reveal critical information about the genetic basis of these conditions. By focusing on the genomics aspects of mitochondrial disorders, researchers can work towards early detection, prevention, and personalized treatment strategies. Genet provides an array of services to support the investigation of genetic factors contributing to mitochondrial disorders, promoting advancements in diagnosis, management, and treatment.
Newborn screening panels aim to identify genetic disorders early in life , allowing for timely intervention and improved health outcomes. The use of genomics in newborn screening can facilitate the detection of a broad range […]
Investigating the genetic factors associated with nervous system diseases can provide valuable insights into the development and progression of these conditions affecting the brain, spinal cord, and peripheral nerves. Genomic research can facilitate early detection, […]