Early-Onset Epileptic Encephalopathy with Phospholipase C Beta 1 Deficiency
The clinical presentation and evolution of epileptic encephalopathy associated with a loss-of-function mutation in the phospholipase C-b 1 gene are reported in a male infant with infantile spasms treated at the University of Birmingham School of Medicine, UK.
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pediatric Neurology Briefs Publishers
2010-12-01
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| coleção: | Pediatric Neurology Briefs |
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| Acesso em linha: | https://www.pediatricneurologybriefs.com/articles/715 |
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