Genomics Research to Elucidate the Genetics of Rare Disease (GREGoR) Renewal

Explore the renewal of the Genomics Research to Elucidate the Genetics of Rare Disease (GREGoR) program in this 25-minute presentation by Lisa Chadwick at the 103rd Meeting of National Advisory Council for Human Genome Research. Gain insights into the National Human Genome Research Institute's efforts to advance rare disease research through genomics. Learn about the program's objectives, potential updates, and its role in uncovering the genetic basis of rare disorders. Understand how this renewal aims to further support scientists in their quest to improve diagnosis and treatment options for patients affected by rare genetic conditions.