Genetic Screening of Frontotemporal Dementia Patients from a Memory Clinic in Argentina
Here we report the genetic screening of familial FTD cases from a memory clinic in Argentina. C9-HRE is still the most common cause of familial FTD. Further studies are warranted on the role of the PSEN2 and PDE11A variants found in two probands. This work adds to the knowledge of the genetic landscape of FTD in our country.
Authors
- Pablo Bagnati (ORCID: https://orcid.org/0000-0003-2801-0537)
- Ezequiel Surace (ORCID: https://orcid.org/0000-0001-8492-9578)
- A. Ojeda
- Ricardo Allegri (ORCID: https://orcid.org/0000-0001-7166-1234)
- Gustavo Emilio Sevlever (ORCID: https://orcid.org/0000-0002-9567-7553)
- Jorge Campos (ORCID: https://orcid.org/0000-0002-1117-1572)
- Nahuel Magrath Guimet (ORCID: https://orcid.org/0000-0002-7420-8547)
Institutions
- Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
- Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (AR)
Publication Details
- Journal
- Alzheimer s & Dementia
- Published
- 2024-12-01
- DOI
- https://doi.org/10.1002/alz.085944
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00