Lack of evidence for an association between UCHL1 S18Y and Parkinson’s disease

UCHL1 has been proposed as a candidate gene for Parkinson’s disease (PD). A meta-analysis of white and Asian subjects reported an inverse association between the non-synonymous UCHL1 S18Y polymorphism and PD risk. However, this finding was not replicated in a large case–control study and updated met...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Hutter, Carolyn M., Samii, Ali, Factor, Stewart A., Nutt, John G., Higgins, Donald S., Bird, Thomas D., Griffith, Alida, Roberts, John W., Leis, Berta C., Montimurro, Jennifer S., Kay, Denise M., Edwards, Karen L., Payami, Haydeh, Zabetian, Cyrus P.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2007
Θέματα:
Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2823263/
https://ncbi.nlm.nih.gov/pubmed/18093156
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1468-1331.2007.02012.x
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