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Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease
Creutzfeldt-Jakob disease (CJD) is a rare transmissible neurodegenerative disorder. The etiology of sporadic form of CJD remains unsolved. In addition to the codon 129 polymorphism, polymorphisms in the non-coding region of PRNP are considered as important factors in sCJD development. To assess a po...
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| Main Authors: | , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Landes Bioscience
2012
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3609072/ https://ncbi.nlm.nih.gov/pubmed/22895088 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.21773 |
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