Nalaganje...
Epilepsy phenotype in patients with Xp22.31 microduplication
The clinical significance of Xp22.31 microduplication is still unclear. We describe a family in which a mother and two children have Xp22.31 microduplication associated with different forms of epilepsy and epileptiform EEG abnormalities. The proband had benign epilepsy with centrotemporal spikes wit...
Shranjeno v:
| izdano v: | Epilepsy Behav Case Rep |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2018
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6310737/ https://ncbi.nlm.nih.gov/pubmed/30603611 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebcr.2018.10.004 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|