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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書誌詳細
出版年:Mol Genet Genomic Med
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2016
主題:
Original Articles
オンライン･アクセス: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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