Beyond SCN1A: genetic diversity in Dravet syndrome-like phenotype and the path to precision treatment.

Datta AN

DOI: 10.1038/s41390-026-04987-5
Published: 2026 Apr 17
Container: Pediatric research
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1038/s41390-026-04987-5,
  title = {Beyond SCN1A: genetic diversity in Dravet syndrome-like phenotype and the path to precision treatment.},
  author = {Datta AN},
  year = {2026},
  journal = {Pediatric research},
  doi = {10.1038/s41390-026-04987-5},
  url = {https://doi.org/10.1038/s41390-026-04987-5}
}

RIS

TY  - JOUR
TI  - Beyond SCN1A: genetic diversity in Dravet syndrome-like phenotype and the path to precision treatment.
AU  - Datta AN
PY  - 2026
JO  - Pediatric research
DO  - 10.1038/s41390-026-04987-5
UR  - https://doi.org/10.1038/s41390-026-04987-5
ER  -

APA

AN, D. (2026). Beyond SCN1A: genetic diversity in Dravet syndrome-like phenotype and the path to precision treatment.. Pediatric research. https://doi.org/10.1038/s41390-026-04987-5

Source records

pubmed · retrieved 2026-09-26T12:26:53.035Z
europe-pmc · retrieved 2026-09-26T12:26:53.083Z