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Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
BACKGROUND: Human prion diseases are relentlessly progressive neurodegenerative disorders which include sporadic Creutzfeldt-Jakob disease (sCJD) and variant CJD (vCJD). Aside from variants of the prion protein gene (PRNP) replicated association at genome-wide levels of significance has proven elusi...
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| 出版年: | BMC Med Genet |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4823897/ https://ncbi.nlm.nih.gov/pubmed/27055460 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0278-2 |
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