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, prevention, and the development of personalized and precision medicine approaches. Genet offers a variety of services to support research in this area, promoting advancements in understanding the genetic factors underlying nervous system diseases and enabling the development of targeted therapies.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
This page represents genomic investigations available for a diverse array of genetic conditions that affect infants and children from birth or shortly thereafter. By studying the genetics and genomics of these disorders, researchers can identify […]
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, […]
Digestive System Diseases
Digestive system diseases involve conditions that affect the gastrointestinal tract and related organs. By exploring the genetic and genomic aspects of these diseases, researchers can uncover the underlying genetic factors that contribute to disease onset […]