Publication | Closed Access
Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor (OXTR) gene: An exploratory study
30
Citations
50
References
2016
Year
Exploratory StudyCongenital ProsopagnosiaDevelopmental AnomalyDevelopmental BiologyGeneticsPhysiologyMorphogenesisCongenital Heart DefectCongenital Heart AnomalyMedicineOxytocin ReceptorEmbryology
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