Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor (OXTR) gene: An exploratory study.
about
P2860
Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor (OXTR) gene: An exploratory study.
description
2016 nî lūn-bûn
@nan
2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Congenital prosopagnosia is as ...... R) gene: An exploratory study.
@ast
Congenital prosopagnosia is as ...... R) gene: An exploratory study.
@en
Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor
@nl
type
label
Congenital prosopagnosia is as ...... R) gene: An exploratory study.
@ast
Congenital prosopagnosia is as ...... R) gene: An exploratory study.
@en
Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor
@nl
prefLabel
Congenital prosopagnosia is as ...... R) gene: An exploratory study.
@ast
Congenital prosopagnosia is as ...... R) gene: An exploratory study.
@en
Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor
@nl
P2093
P1433
P1476
Congenital prosopagnosia is as ...... TR) gene: An exploratory study
@en
P2093
Boris Suchan
Federico Manai
Manuela Malaspina
Mariarita Lillo
Sergio Comincini
Susanna Schiavi
Valentina Fermi
Zaira Cattaneo
P304
P356
10.1016/J.NEUROSCIENCE.2016.09.040
P407
P577
2016-09-28T00:00:00Z