Lack of Association between PRNP M129V Polymorphism and Multiple Sclerosis, Mild Cognitive Impairment, Alcoholism and Schizophrenia in a Korean Population

The genetic variant at codon 129 (M129V) of the prion protein gene (PRNP) is considered to be a major genetic risk factor for prion diseases. In this study, we examined the possible genetic association of PRNP*129Val with multiple sclerosis (MS, n = 681), mild cognitive impairment (MCI, n = 801), al...

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Bibliografiset tiedot
Päätekijät: Choi, Ihn-Geun, Woo, Sung-Il, Kim, Ho Jin, Kim, Dai-Jin, Park, Byung Lae, Cheong, Hyun Sub, Pasaje, Charisse Flerida A., Park, Tae Joon, Bae, Joon Seol, Chai, Young Gyu, Shin, Hyoung Doo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: IOS Press 2010
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Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3833710/
https://ncbi.nlm.nih.gov/pubmed/20592456
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/DMA-2010-0711
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