“…The deficit occurs in both sporadic AD and familial AD caused by a specific genetic mutation, as well as in asymptomatic carriers of the mutation (Liang et al ., ; Parra, Abrahams, Logie, & Della Sala, ). This binding deficit has been proposed as a diagnostic tool since it allows differentiation between AD and other forms of dementia and clinical conditions (Cecchini et al ., ; Della Sala, Parra, Fabi, Luzzi, & Abrahams, ; Liang et al ., ; Parra, ; Parra, Abrahams, Logie, & Della Sala, ).…”