Trailblazing study discovers novel genetic causes of rare diseases, leading to improved diagnosis and better patient care

A research programme pioneering the use of whole genome sequencing in the NHS has diagnosed hundreds of patients and discovered new genetic causes of disease.
Source: University of Bristol news - Category: Universities & Medical Training Tags: Health, Research; Faculty of Biomedical Sciences, School of Cellular and Molecular Medicine, Faculty of Health Sciences, Bristol Medical School, Faculty of Health Sciences, Translational Health Sciences; Press Release Source Type: news