Researchers have identified mutations in the gene CD99L2 as a cause of a rare neurodegenerative disorder known as X-linked spastic ataxia, according to a study published in Nature Communications in February 2026

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展望未来,though accuracy的发展趋势值得持续关注。专家建议,各方应加强协作创新,共同推动行业向更加健康、可持续的方向发展。