Single point mutation on the gene encoding dysbindin results in recognition deficits.
Autor: | Chang, E. H.1,2,3,4 echang1@northwell.edu, Fernando, K.1,2, Yeung, L. W. E.1,2, Barbari, K.1,2, Chandon, T.-S. S.1,2, Malhotra, A. K.1,2,3,4 |
---|---|
Zdroj: | Genes, Brain & Behavior. Jun2018, Vol. 17 Issue 5, p1-9. 9p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |