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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Publicat a:Neurology
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Lippincott Williams & Wilkins 2016
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Article
Accés en línia: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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