Loading...
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...
Na minha lista:
| Udgivet i: | Front Biol (Beijing) |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2017
|
| Fag: | |
| Online adgang: | 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 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|