Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5–6.0 Hz polyspike waves

Juvenile myoclonic epilepsy (JME), the most common genetic epilepsy, remains enigmatic because it is considered one disease instead of several diseases. We ascertained three large multigenerational/multiplex JME pedigrees from Honduras with differing JME subsyndromes, including Childhood Absence Epi...

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Detalles Bibliográficos
Autores principales: Wight, Jenny E., Nguyen, Viet‐Huong, Medina, Marco T., Patterson, Christopher, Durón, Reyna M., Molina, Yolly, Lin, Yu‐Chen, Martínez‐Juárez, Iris E., Ochoa, Adriana, Jara‐Prado, Aurelio, Tanaka, Miyabi, Bai, Dongsheng, Aftab, Sumaya, Bailey, Julia N., Delgado‐Escueta, Antonio V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799870/
https://www.ncbi.nlm.nih.gov/pubmed/27066514
http://dx.doi.org/10.1002/mgg3.195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799870/
https://www.ncbi.nlm.nih.gov/pubmed/27066514
http://dx.doi.org/10.1002/mgg3.195

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