Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.

BMC Med Genet · 2013 · PMC3847123 · PMID 24028506

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highly significantno p-value reported

Conclusions These data provide the first highly significant confirmation of SNP allele frequencies for a novel CJD candidate gene providing new avenues for investigating these neurodegenerative prion diseases.

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