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  • De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

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Research Article
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

Authors

    Citation

    Dumanchin C, Brice A, Campion D, et al
    De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.
    Journal of Medical Genetics 1998;35:672-673.

    Publication history

    • First published August 1, 1998.
    Online issue publication 
    April 27, 2016

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