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Your donations help advance our goals
We support research aimed at accelerating the understanding of CLCN4 biology, to allow identification of effective new treatments. This is an emerging space with much potential to make a difference.
We work to raise awareness of CLCN4 as a condition amongst geneticists, neurologists and scientists. This improves rates of diagnosis and accelerates the momentum for research.
Patients with CLCN4 gene variants can suffer from developmental delay, seizures, and behavioural challenges. We understand how having a loved one with this condition can be life-changing. We are here to support you, and to develop treatments that enhance quality of life in the areas that matter.
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