Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

OBJECTIVE: To generate a clinical and pathologic phenotype of patients carrying rare loss-of-function mutations in ABCA7, identified in a Belgian Alzheimer patient cohort and in an autosomal dominant family. METHODS: We performed a retrospective review of available data records, medical records, res...

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Vydáno v:Neurology
Hlavní autoři: Van den Bossche, Tobi, Sleegers, Kristel, Cuyvers, Elise, Engelborghs, Sebastiaan, Sieben, Anne, De Roeck, Arne, Van Cauwenberghe, Caroline, Vermeulen, Steven, Van den Broeck, Marleen, Laureys, Annelies, Peeters, Karin, Mattheijssens, Maria, Vandenbulcke, Mathieu, Vandenberghe, Rik, Martin, Jean-Jacques, De Deyn, Peter P., Cras, Patrick, Van Broeckhoven, Christine
Médium: Artigo
Jazyk:Inglês
Vydáno: Lippincott Williams & Wilkins 2016
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4917260/
https://ncbi.nlm.nih.gov/pubmed/27037232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000002628
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