多基因风险评分与患多发性硬化症的终身风险在基于人口的出生年龄队列中的关联

Floor C Loonstra1, Daniel Álvarez Sirvent1, Niccoló Tesi1

  • 1From the MS Center Amsterdam (F.C.L., E.M.M.S., B.U.), Neurology, Amsterdam Neuroscience, Genomics of Neurodegenerative Diseases and Aging (D.Á.S., N.T., H.H., A.N.S., M.H., S.J.V.D.L.), Human Genetics, and Alzheimer Center Amsterdam (H.H., S.J.V.D.L.), Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc; Delft Bioinformatics Lab (N.T., H.H.), Delft University of Technology; and Amsterdam Neuroscience (H.H., S.J.V.D.L.), Neurodegeneration, the Netherlands.

Neurology
|September 13, 2024
PubMed
概括

遗传因素显著影响多发性硬化症 (MS) 的终身风险. 高的多基因风险分数 (PRS) 会增加MS的可能性,而低的PRS可能表明其他疾病,有助于诊断.

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