Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

Alzheimer disease (AD) is a progressive neurodegenerative disorder and the most common form of dementia. The majority of AD cases are sporadic, while up to 5% are families with an early onset AD (EOAD). Mutations in one of the three genes: amyloid beta precursor protein (APP), presenilin 1 (PSEN1) o...

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Detalles Bibliográficos
Autores principales: Thonberg, Håkan, Chiang, Huei-Hsin, Lilius, Lena, Forsell, Charlotte, Lindström, Anna-Karin, Johansson, Charlotte, Björkström, Jenny, Thordardottir, Steinunn, Sleegers, Kristel, Van Broeckhoven, Christine, Rönnbäck, Annica, Graff, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465543/
https://www.ncbi.nlm.nih.gov/pubmed/28595629
http://dx.doi.org/10.1186/s40478-017-0441-9

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