De novo SCN1A missense variant in a patient with Parkinson’s disease

Majed Alluqmani, Abdulfatah M. Alayoubi, Jamil A. Hashmi, Sulman Basit

Open source

DOI: 10.3389/fgene.2024.1496683
Published: 2024-11-06
Container: Frontiers in Genetics
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fgene.2024.1496683,
  title = {De novo SCN1A missense variant in a patient with Parkinson’s disease},
  author = {Majed Alluqmani and Abdulfatah M. Alayoubi and Jamil A. Hashmi and Sulman Basit},
  year = {2024},
  journal = {Frontiers in Genetics},
  doi = {10.3389/fgene.2024.1496683},
  url = {https://doi.org/10.3389/fgene.2024.1496683}
}

RIS

TY  - JOUR
TI  - De novo SCN1A missense variant in a patient with Parkinson’s disease
AU  - Majed Alluqmani
AU  - Abdulfatah M. Alayoubi
AU  - Jamil A. Hashmi
AU  - Sulman Basit
PY  - 2024
JO  - Frontiers in Genetics
DO  - 10.3389/fgene.2024.1496683
UR  - https://doi.org/10.3389/fgene.2024.1496683
ER  -

APA

Alluqmani, M., Alayoubi, A. M., Hashmi, J. A., & Basit, S. (2024). De novo SCN1A missense variant in a patient with Parkinson’s disease. Frontiers in Genetics. https://doi.org/10.3389/fgene.2024.1496683

Source records

crossref · retrieved 2026-09-25T03:09:53.382Z