Kcnt1 Slack Epilepsy Foundation Inc
Variants in the KCNT1 gene cause drug-resistant seizures. Support us in finding new treatments! The mission of the KCNT1 Epilepsy Foundation is to support research and drug development efforts focused on finding a cure for KCNT1-related pediatric epilepsy. The KCNT1 Epilepsy Foundation supports the KCNT1 community with educational resources and the latest research information.
Founded
2019
1376
Web
kcnt1epilepsy.org
Address
Scottsdale
KCNT1 Epilepsy Foundation - Hope is on the Horizon Hope is on the horizon The mission of the KCNT1 Epilepsy Foundation is to bring people together with KCNT1 gene variants and accelerateresearch and drug development efforts focused on findinga cure for KCNT1related epilepsy. The KCNT1 Epilepsy Foundation is here to support the KCNT1 community with educational resources and the latest research information. What can a kcnt1 gene variant cause. In some people KCNT1 gene variants can lead to KCNT1related epilepsy.
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Together, we can make a real impact in communities around the world. Help us bring hope and support.
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Discussions
Odpovědí v diskuzi
1
1. How can we enhance collaboration between families, clinicians, and researchers to accelerate the development of new treatments for KCNT1-related epilepsy?
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Brooklyn Simmons
2 days ago
Odpovědí v diskuzi
1
2. What role do you think community awareness and education play in supporting individuals with KCNT1 gene variants and their families?
View
Brooklyn Simmons
2 days ago
Latest reviews
Together, we can make a real impact in communities around the world. Help us bring hope and support.
💙 Grateful for the work you do! Together, we can raise awareness and support families impacted by KCNT1-related epilepsy. Hope really is on the horizon! 🌟
Brooklyn Simmons
Product Manager
👏 Thank you, KCNT1 Epilepsy Foundation, for being a lifeline for so many! Your efforts in research and support are truly inspiring. Let’s keep pushing for breakthroughs! #EndEpilepsy 💪
Brooklyn Simmons
Product Manager
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