Wordt geladen...
Epilepsy in Muenke Syndrome: FGFR3-Related Craniosynostosis
Epilepsy, a neurologic disorder characterized by the predisposition to recurrent unprovoked seizures, is reported in more than 300 genetic syndromes. Muenke syndrome is an autosomal-dominant craniosynostosis syndrome characterized by unilateral or bilateral coronal craniosynostosis, hearing loss, in...
Bewaard in:
| Hoofdauteurs: | , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2012
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4133743/ https://ncbi.nlm.nih.gov/pubmed/23044018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2012.07.004 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|