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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Blindness and OXTR[original query]
Congenital prosopagnosia is associated with a genetic variation in the oxytocin receptor (OXTR) gene: An exploratory study.
Neuroscience 2016 Sep .
Cattaneo Zaira, Daini Roberta, Malaspina Manuela, Manai Federico, Lillo Mariarita, Fermi Valentina, Schiavi Susanna, Suchan Boris, Comincini Serg
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