Mitochondrial diseases (MDs) encompass a diverse range of genetically heterogeneous disorders arising from dysfunctional mitochondria. Given the broad impact of mitochondrial dysfunctions on vital organs with high energy demands, including the liver, skeletal and cardiovascular muscles, as well as the brain, MDs present numerous challenges in terms of diagnosis, therapeutic, and research. Recognizing the paramount significance of every facet of research in this field, Protheragen has assembled a team comprising passionate experts dedicated to delivering cutting-edge solutions.
Featured Solutions
By Disease
We provide research services for different types of mitochondrial diseases.
By Applications
We offer a range of diagnostic and therapeutic development services.
By Molecular Type
We provide therapeutic development services for various molecular types.
Our Advantages
Whether you are seeking diagnostic development support or therapeutic development for a specific mitochondrial disease, Protheragen offers a comprehensive range of services. Our expertise spans from the development of genetic markers to drug screening and preclinical studies. Our dedicated team will collaborate with you to ensure optimal progress for your project. Please feel free to contact us if needed.