Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis.

Int J Mol Sci · 2022 · PMC9570223 · PMID 36232761

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nominally significantno p-value reported

The missense variants in PRAM1 and USH2A showed nominally significant association with MS in the exome chip study of the IMSGC [ 24 ].

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