A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis. (Q49063531)

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A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis.
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    A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis. (English)

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