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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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2016
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4799870/
https://ncbi.nlm.nih.gov/pubmed/27066514
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.195
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