CURE ADSSL1
501(c)(3) non-profit patient advocacy group with the mission to find treatment for ADSSL1 myopathy Mission of the CURE ADSSL1 organization is to invest in research and develop treatment options for patients with rare neuromuscular disease caused by mutation in ADSSL1 gene. We have a patient community that supports each other in sharing knowledge to help manage disease symptoms and quality of life.
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Glendale
Cure for ADSSL1 gene myopathy Striving for Treatment For ADSSL1 Myopathy Patients We are working with leading medical researchers and rare disease experts to develop a treatment for patients with neuromuscular disease caused by an inborn error of purine metabolism due to mutation in the ADSSL1 gene. Striving for Treatment For ADSSL1 Myopathy Patients We are working with leading medical researchers and rare disease experts to develop a treatment for patients with neuromuscular disease caused by an inborn error of purine metabolism due to mutation in the ADSSL1 gene. Striving for Treatment For ADSSL1 Myopathy Patients We are working with leading medical researchers and rare disease experts to develop a treatment for patients with neuromuscular disease caused by an inborn error of purine metabolism due to mutation in the ADSSL1 gene. About Our Organization We are a patientled nonprofit organization with the mission to find a cure for ADSSL1 Myopathy a rare neuromuscular disease caused by an inborn error of purine metabolism due to mutation in the ADSSL1 gene.
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