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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: 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
פורמט: Artigo
שפה:Inglês
יצא לאור: BioMed Central 2010
נושאים:
Research Article
גישה מקוונת: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
תגים: הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

פריטים דומים