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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Detalles Bibliográficos
Autores principales: Kim, Hak-Jae, Park, Jin Kyung, Kim, Su Kang, Kang, Sung Wook, Kim, Jong Woo, Park, Hyun-Kyung, Cho, Ah-Rang, Song, Ji Young, Chung, Joo-Ho
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887425/
https://www.ncbi.nlm.nih.gov/pubmed/20492734
http://dx.doi.org/10.1186/1471-2350-11-78

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887425/
https://www.ncbi.nlm.nih.gov/pubmed/20492734
http://dx.doi.org/10.1186/1471-2350-11-78

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