Evolution from reflex myoclonic epilepsy of infancy to childhood absence epilepsy in <scp>NRXN1</scp> ‐related disorder

Shanine Kamgang, Kenneth A. Myers

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DOI: 10.1002/epd2.70409
Published: 2026-09-12
Container: Epileptic Disorders
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1002/epd2.70409,
  title = {Evolution from reflex myoclonic epilepsy of infancy to childhood absence epilepsy in
                    <scp>NRXN1</scp>
                    ‐related disorder},
  author = {Shanine Kamgang and Kenneth A. Myers},
  year = {2026},
  journal = {Epileptic Disorders},
  doi = {10.1002/epd2.70409},
  url = {https://doi.org/10.1002/epd2.70409}
}

RIS

TY  - JOUR
TI  - Evolution from reflex myoclonic epilepsy of infancy to childhood absence epilepsy in
                    <scp>NRXN1</scp>
                    ‐related disorder
AU  - Shanine Kamgang
AU  - Kenneth A. Myers
PY  - 2026
JO  - Epileptic Disorders
DO  - 10.1002/epd2.70409
UR  - https://doi.org/10.1002/epd2.70409
ER  -

APA

Kamgang, S., & Myers, K. A. (2026). Evolution from reflex myoclonic epilepsy of infancy to childhood absence epilepsy in <scp>NRXN1</scp> ‐related disorder. Epileptic Disorders. https://doi.org/10.1002/epd2.70409

Source records

crossref · retrieved 2026-09-25T07:10:01.932Z