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    Incomplete penetrance in familial Alzheimer’s disease with PSEN1 Ala260Gly mutation

    Presenilin1 (PSEN1) gene is the most common known genetic cause of early-onset familial Alzheimer’s disease. We describe an Italian family with the known p.Ala260Gly mutation in PSEN1 gene. The presence of an ...

    I. Piaceri, A. Chiari, C. Galli, S. Bagnoli, C. Ferrari… in Neurological Sciences (2020)