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Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity
BACKGROUND: Familial cerebral cavernous malformation type 1 (CCM1) is an autosomal dominant disease caused by mutations in the Krev Interaction Trapped 1 (KRIT1/CCM1) gene, and characterized by multiple brain lesions that often result in intracerebral hemorrhage (ICH), seizures, and neurological def...
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| Publicado no: | Cerebrovasc Dis |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4297571/ https://ncbi.nlm.nih.gov/pubmed/25472749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000369200 |
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