With our personalized screening services, we seek to understand both the impact of an individual’s genetic mutation on cellular function and the effects of different drugs in a laboratory model of the mutation.
Here’s what we do to arrive at these scientific insights:
We provide the individual’s physician with informational reports that summarize these findings.
- The cellular characterization report describes the normal cellular processes that are disrupted by the individual’s mutation.
- The drug screening report describes the activities of different drugs at the cellular level using laboratory models.
These documents provide details on the data we generated and the methods we used in our research. Pairnomix does not offer any recommendations based on our findings in these reports.
Pairnomix is able to perform these services for individuals with mutations in a wide array of genes implicated in rare central nervous system disorders. The costs and time requirements for our work are determined by the type of scientific research needed for a particular genetic mutation.
Please contact us if you are interested in having these services performed for a specific genetic mutation. Our Patient Advocacy Team will be happy to speak with you about the process, cost, and answer any questions you might have.