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

✍ Scribed by P. E. Jiménez Caballero; C. De Diego Boguna; E. Martin Correa; M. Serviá Candela; C. Marsal Alonso

No coin nor oath required. For personal study only.

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