Unusual phenotypic alteration of β amyloid precursor protein (βAPP) maturation by a new Val-715 → Met βAPP-770 mutation responsible for probable early-onset Alzheimer’s disease...

Por Ancolio, K., Dumanchin, C., Barelli, H., Warter, J. M., Brice, A., Campion, D., Frébourg, T., Checler, F.
Publicado em 1999

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

Por Dumanchin, C, Brice, A, Campion, D, Hannequin, D, Martin, C, Moreau, V, Agid, Y, Martinez, M, Clerget-Darpoux, F, Frebourg, T
Publicado em 1998

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

Por Campion, D, Dumanchin, C, Hannequin, D, Dubois, B, Belliard, S, Puel, M, Thomas-Anterion, C, Michon, A, Martin, C, Charbonnier, F, Raux, G, Camuzat, A, Penet, C, Mesnage, V, Martinez, M, Clerget-Darpoux, F, Brice, A, Frebourg, T
Publicado em 1999