Phenotypic and Genotypic Characterization of NPRL2-Related Epilepsy: Two Case Reports and Literature Review

The phenotype of nitrogen permease regulator-like 2 (NPRL2) gene-related epilepsy clinically manifests as a range of epilepsy syndromes, including familial focal epilepsy with variable foci (FFEVF), sleep-related hypermotor epilepsy (SHE), temporal lobe epilepsy (TLE), frontal lobe epilepsy (FLE), a...

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Detalles Bibliográficos
Autores principales: Sun, Yulin, Wan, Lin, Yan, Huimin, Li, Zhichao, Yang, Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8667312/
https://www.ncbi.nlm.nih.gov/pubmed/34912289
http://dx.doi.org/10.3389/fneur.2021.780799

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8667312/
https://www.ncbi.nlm.nih.gov/pubmed/34912289
http://dx.doi.org/10.3389/fneur.2021.780799

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