Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes

Early-onset dementia (EOD), with symptom onset before age 65, has a strong genetic burden. Due to genetic and clinical overlaps between different types of dementia, whole-exome sequencing (WES) has emerged as an appropriate screening method for diagnostic testing and novel gene-finding approaches. W...

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Detalles Bibliográficos
Autores principales: Silvaieh, Sara, König, Theresa, Wurm, Raphael, Parvizi, Tandis, Berger-Sieczkowski, Evelyn, Goeschl, Stella, Hotzy, Christoph, Wagner, Matias, Berutti, Riccardo, Sammler, Esther, Stögmann, Elisabeth, Zimprich, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276391/
https://www.ncbi.nlm.nih.gov/pubmed/37330543
http://dx.doi.org/10.1186/s40246-023-00499-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276391/
https://www.ncbi.nlm.nih.gov/pubmed/37330543
http://dx.doi.org/10.1186/s40246-023-00499-z

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