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Molecular and genetic insights into an infantile epileptic encephalopathy – CDKL5 disorder
BACKGROUND: The discovery that mutations in cyclin-dependent kinase-like 5 (CDKL5) gene are associated with infantile epileptic encephalopathy has stimulated world-wide research effort to understand the molecular and genetic basis of CDKL5 disorder. Given the large number of literature published thu...
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| Yayımlandı: | Front Biol (Beijing) |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5453648/ https://ncbi.nlm.nih.gov/pubmed/28580010 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11515-016-1438-7 |
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