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
Eye Diseases
Eye diseases encompass a range of conditions that affect the structure and function of the eyes. By studying the genetic and genomic aspects of these diseases, researchers can gain a deeper understanding of the underlying […]
Genetic Disease Research
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 […]
Genetic Disease Research
Male Urogenital Diseases
Male urogenital diseases encompass a variety of conditions affecting the male reproductive and urinary systems. Delving into the genetic and genomic aspects of these diseases can shed light on the genetic factors that contribute to […]