Identification of Non-coding Pathogenic Variants for Rare Disease Colloquium - Kickoff Symposium
This colloquium series is designed to build community and unite expertise around the genetic causes of rare mendelian disease, specifically identifying pathogenic non-coding mutations in rare pediatric diseases.
The Kickoff Symposium leverages Duke-unique capabilities and features presentations from leading experts of clinical, experimental, and quantitative perspectives. Each session will include a summary of current research capabilities, outstanding questions, as well as an opportunity for open discussion. The day will conclude with dinner and continued exploration of collaborative opportunities.
The cross discipline agenda will optimize opportunities for external funding, and ultimately scientific achievement in the area of pediatric rare
diseases and gene regulation.