Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor (OXTR) gene: An exploratory study

Zaira Cattaneo, Roberta Daini, Manuela Malaspina, Federico Manai, Mariarita Lillo, Valentina Fermi, Susanna Schiavi, Boris Suchan, Sergio Comincini

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Medicine & Life Sciences