WITH INVITAE, YOU’RE PART OF THE SOLUTION
Thanks to people like you, the experience of living with genetic conditions can be understood like never before. The more health information we collect through patient surveys and uploaded medical reports, the closer we can get to helping communities find treatments that work.
The KCNQ2 PIN will organize a system of information that will use observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for KCNQ2 epileptic mutations.
The KCNQ2 registry can offer adaptable designs and data collection strategies, making them particularly useful as treatments rapidly change. The registry will reveal crucial data for scientists that will speed up the development of drugs and new treatments for individuals with KCNQ2 mutations.
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