A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis. (Q49063531)
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English | A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis. |
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Statements
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A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis. (English)
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P E Jiménez Caballero
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A Lladó
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C de Diego Boguna
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E Martin Correa
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M Serviá Candela
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C Marsal Alonso
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15 July 2008
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15
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991-994
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9
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Identifiers
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