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No association between polymorphisms of WNT2 and schizophrenia in a Korean population
BACKGROUND: Wingless-type MMTV integration site family member 2 (WNT2) has a potentially important role in neuronal development; however, there has yet to be an investigation into the association between single nucleotide polymorphisms (SNPs) of WNT2 and schizophrenia. This study aimed to determine...
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| Main Authors: | , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2010
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2887425/ https://ncbi.nlm.nih.gov/pubmed/20492734 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-78 |
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