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Association of Genetic Variations in X‐Ray Repair Cross‐Complementing Group 1 and Tourette Syndrome
BACKGROUND: X‐ray repair cross‐complementing group 1 (XRCC1) plays a central role in mammalian DNA repair process. The polymorphism rs25487 (Arg>Gln at codon 399) of this gene is common in Han Chinese population. OBJECTIVES: The objective of this study was to analyze the association between this...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Clin Lab Anal |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807472/ https://ncbi.nlm.nih.gov/pubmed/23001975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21525 |
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