De novo SCN1A missense variant in a patient with Parkinson’s disease
Our results suggest that the pathogenic variant in <i>SCN1A</i> may lead to PD features without epilepsy.
Authors
- Abdulfatah M. Alayoubi (ORCID: https://orcid.org/0000-0001-9250-940X)
- Jamil Amjad Hashmi (ORCID: https://orcid.org/0000-0001-8598-8799)
- Sulman Basit (ORCID: https://orcid.org/0000-0003-4294-6825)
- Majed Alluqmani (ORCID: https://orcid.org/0000-0002-5416-6247)
Institutions
- Taibah University (SA)
Publication Details
- Journal
- Frontiers in Genetics
- Published
- 2024-11-06
- DOI
- https://doi.org/10.3389/fgene.2024.1496683
- Primary Topic
- Epilepsy research and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- King Salman Center for Disability Research