De Novo KCNB1 Mutations in Epileptic Encephalopathy

BACKGROUND: Numerous studies have demonstrated increased load of de novo copy number variants (CNVs) or single nucleotide variants (SNVs) in individuals with neurodevelopmental disorders, including epileptic encephalopathies, intellectual disability and autism. METHODS: We searched for de novo mutat...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Torkamani, Ali, Bersell, Kevin, Jorge, Benjamin S., Bjork, Robert L., Friedman, Jennifer R., Bloss, Cinnamon S., Cohen, Julie, Gupta, Siddharth, Naidu, Sakkubai, Vanoye, Carlos G., George, Alfred L., Kearney, Jennifer A.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2014
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4192091/
https://ncbi.nlm.nih.gov/pubmed/25164438
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24263
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