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• Groundbreaking Discovery Of CD99L2 Gene Variants Solves Genetic Mystery Of X Linked Spastic Ataxia

  Published: Mar 17, 2026

  Section: Science & Tech

  A collaborative study between researchers in Bochum and Tübingen has identified the CD99L2 gene as a primary driver of rare movement disorders. By analyzing a cohort of nearly 3,00...

• Scientific Breakthrough Identifies CD99L2 Gene as Primary Cause of Rare X-Linked Spastic Ataxia

  Published: Mar 17, 2026

  Section: Science & Tech

  A joint research team from Bochum and Tübingen has pinpointed disease causing variants of the CD99L2 gene in a massive cohort of 2,811 patients. The study, published in Nature Comm...