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Young Onset Alzheimer’s Disease Associated with C9ORF72 Hexanucleotide Expansion: Further Evidence for a Still Unsolved Association

Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are recognized as part of a disease continuum (FTD-ALS spectrum), in which the most common genetic cause is chromosome 9 open reading frame 72 (C9ORF72) gene hexanucleotide repeat expansion. The clinical phenotype of patients carr...

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Detalles Bibliográficos
Autores principales:	Vinceti, Giulia, Gallingani, Chiara, Zucchi, Elisabetta, Martinelli, Ilaria, Gianferrari, Giulia, Simonini, Cecilia, Bedin, Roberta, Chiari, Annalisa, Zamboni, Giovanna, Mandrioli, Jessica
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138077/ https://www.ncbi.nlm.nih.gov/pubmed/37107688 http://dx.doi.org/10.3390/genes14040930

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