Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management

Esma Şengenç, Şeyma Sönmez Şahin, Akın İşcan, Dilara Füsun İçağasıoğlu, Gözde Yeşil, Ayça Dilruba Aslanger

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DOI
10.65717/turkarchpediatr.2026.26154
Published
2026-07-13
Container
Turkish Archives of Pediatrics
Publisher
Caleo
Open access
unknown

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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

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