riaanresearch.org - Riaan Research Initiative — Cockayne Syndrome

Description: We have the tools to conquer genetic disease. Our mission is to accelerate the development of treatments for Cockayne syndrome.

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Our mission is to accelerate the development of treatments for Cockayne syndrome. We seek to identify, promote, and/or fund intelligent, innovative, and thoughtful research proposals. Such therapies may include gene therapy, gene editing, and/or drug repurposing screens. We invite interested researchers to connect with us by emailing [email protected].

Has your child or loved one been diagnosed with Cockayne syndrome? Register as a Patient Family We envision a world where parents have access to treatments for severe and life-limiting genetic diseases that threaten their children’s lives.

​ We envision a world where all of our children have a chance to grow up to pursue their dreams, to live, to love, to thrive, and most importantly, to feel and be a part of everything beautiful that life, that the human experience, has to offer.

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