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.
Genetic Disease Research
Immune System Diseases
he genetic factors underlying immune system diseases can provide valuable insights into the body’s defense mechanisms and susceptibility to various conditions. Genomic research can facilitate early detection, prevention, and the development of personalized medicine for […]
Genetic Disease Research
Hemic and Lymphatic Diseases
By exploring the genetic components of hemic and lymphatic diseases, researchers can identify key factors that influence blood cells and the lymphatic system. Genomic research in this area can lead to early detection and prevention […]
Genetic Disease Research
Recommended Newborn Screening Panels
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 […]