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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关于Are people,以下几个关键信息值得重点关注。本文结合最新行业数据和专家观点,为您系统梳理核心要点。

首先,2026-03-19 ~17:43 2

Are people

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此外,Medact has highlighted privacy issues in the UK regarding Palantir's access to anonymized patient records. (Anonymization removes direct identifiers like names and national insurance numbers). In its briefing, Medact contended the NHS's data safeguards are inadequate, though NHS England asserts data is anonymized within its national Federated Data Platform. Medact referenced worries that such data could be relatively easily traced back to individuals.

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