Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor (OXTR) gene: An exploratory study
| Autor: | Cattaneo, Zaira, Daini, Roberta, Malaspina, Manuela, Manai, Federico, Lillo, Mariarita, Fermi, Valentina, Schiavi, Susanna, Suchan, Boris, Comincini, Sergio |
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| Zdroj: | In Neuroscience 17 December 2016 339:162-173 |
| Databáze: | ScienceDirect |
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