लोड हो रहा है...
De novo mutations in the classic epileptic encephalopathies
Epileptic encephalopathies (EE) are a devastating group of severe childhood epilepsy disorders for which the cause is often unknown. Here, we report a screen for de novo mutations in patients with two classical EE: infantile spasms (IS, n=149) and Lennox-Gastaut Syndrome (LGS, n=115). We sequenced t...
में बचाया:
| स्वरूप: | Artigo |
|---|---|
| भाषा: | Inglês |
| प्रकाशित: |
2013
|
| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3773011/ https://ncbi.nlm.nih.gov/pubmed/23934111 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature12439 |
| टैग : |
टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
|