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
Endocrine System Diseases
Endocrine system diseases affect the glands and hormones responsible for regulating various bodily functions. Investigating the genetics and genomics of endocrine system diseases can provide valuable insights into the genetic factors that influence these conditions. […]
Genetic Disease Research
Mental Disorders
Examining the genetic components of mental disorders can shed light on the complex interplay between genes and environmental factors in the development and progression of these conditions. Genomics research can contribute to early detection, prevention, […]
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 […]