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Publications
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Giaccone G, Rossi G, Morbin M, Tagliavini F, Bugiani O. A713T mutation of the APP gene in an Italian family with Alzheimer disease and severe congophilic angiopathy. Neurobiology of Aging 23 Supp 1: 320, 2002 |
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APP:
(Ala713Thr)
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ID: 564 | |
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Rossi G, Giaccone G, Maletta R, Morbin M, Capobianco R, Mangieri M, Giovagnoli AR, Bizzi A, Tomaino C, Perri M, Di Natale M, Tagliavini F, Bugiani O, Bruni AC. A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene. Neurology 63: 910-912, 2004 (PubMed ID: 15365148) |
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APP:
(Ala713Thr)
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ID: 342 | |
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Armstrong J, Boada M, Rey MJ, Vidal N, Ferrer I. Familial Alzheimer disease associated with A713T mutation in APP. Neuroscience Letters 370: 241-243, 2004 (PubMed ID: 15488330) |
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APP:
(Ala713Thr)
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ID: 343 | |
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Bernardi L, Geracitano S, Colao R, Puccio G, Gallo M, Anfossi M, Frangipane F, Curcio SA, Mirabelli M, Tomaino C, Vasso F, Smirne N, Maletta R, Bruni AC. AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions. Journal of Alzheimer's Disease 17: 383-389, 2009 (PubMed ID: 19363265) |
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APP:
(Ala713Thr)
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ID: 643 | |
Mutation color legend:
Red: mutation is pathogenic
Orange: pathogenic nature is unclear
Green: mutation is not pathogenic
Selection:
Publication ID In (342,343,564,643)
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