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An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder
We report a three generation pedigree with 11 of 22 affected with a variant form of rolandic epilepsy, speech impairment, oromotor apraxia, and cognitive deficit. The core features comprised nocturnal rolandic seizures, interictal centrotemporal spike waves with early age of onset and late age of of...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2435390/ https://ncbi.nlm.nih.gov/pubmed/18248446 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1528-1167.2007.01517.x |
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