INVESTIGATE
disease mechanisms and novel therapeutic approaches associated with MAPK8IP3 genetic variants
In Pursuit of a Treatment for MAPK8IP3 Genetic Mutation
The Wolverine Foundation
We are committed to promoting positive change by supporting genomics research for ultra-rare diseases, educational initiatives, and support for our armed forces.
ADVANCING RESEARCH. DISCOVERING NOVEL THERAPEUTIC APPROACHES.
We are dedicated to advancing groundbreaking scientific therapies, pioneering medical innovations, and fostering collaborative knowledge to uncover transformative treatments for MAPK8IP3 and potentially other central nervous system (CNS) disorders.
MANAGE
a diverse portfolio of research projects that encourages scientific collaboration to more directly connect academic research, drug discovery and clinical development.
About Us
WE WORK IN A NUMBER OF DIFFERENT WAYS
WHAT IS MAPK8IP3?
The MAPK8IP3-related neurodevelopmental disorder leads to substantial delays in cognitive, motor, and social development for affected individuals.
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WHAT AREAS OF RESEARCH ARE BEING EXPLORED?
The Wolverine Foundation aims to leverage cutting-edge scientific models, medical breakthroughs, and shared knowledge to drive discoveries that will pave the way for effective treatments for MAPK8IP3 and potentially other CNS diseases
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ARE YOU NEWLY DIAGNOSED?
If you or a loved one has recently been diagnosed with MAPK8IP3-related neurodevelopmental disorder, you can find resources here.
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