Join us for a discussion with our scientist panel to learn more about:
The widespread impact of rare diseases (7,000 known rare diseases, 300 million worldwide affected, 50 percent of rare disease patients are children)
How next-generation sequencing has uncovered the genes responsible more than 50 percent of all rare diseases
How the genomic study of rare diseases has advanced the understanding of all diseases
How using cutting-edge methods to analyze genetic variants is responsible for rare disease risks
Details, register here.