Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management
- DOI
- 10.65717/turkarchpediatr.2026.26154
- Published
- 2026-07-13
- Container
- Turkish Archives of Pediatrics
- Publisher
- Caleo
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.65717/turkarchpediatr.2026.26154,
title = {Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management},
author = {Esma Şengenç and Şeyma Sönmez Şahin and Akın İşcan and Dilara Füsun İçağasıoğlu and Gözde Yeşil and Ayça Dilruba Aslanger},
year = {2026},
journal = {Turkish Archives of Pediatrics},
doi = {10.65717/turkarchpediatr.2026.26154},
url = {https://doi.org/10.65717/turkarchpediatr.2026.26154}
}RIS
TY - JOUR TI - Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management AU - Esma Şengenç AU - Şeyma Sönmez Şahin AU - Akın İşcan AU - Dilara Füsun İçağasıoğlu AU - Gözde Yeşil AU - Ayça Dilruba Aslanger PY - 2026 JO - Turkish Archives of Pediatrics DO - 10.65717/turkarchpediatr.2026.26154 UR - https://doi.org/10.65717/turkarchpediatr.2026.26154 ER -
APA
Şengenç, E., Şahin, Ş. S., İşcan, A., İçağasıoğlu, D. F., Yeşil, G., & Aslanger, A. D. (2026). Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management. Turkish Archives of Pediatrics. https://doi.org/10.65717/turkarchpediatr.2026.26154
Source records
- crossref · retrieved 2026-09-26T10:42:28.733Z