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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Bibliografiske detaljer
Udgivet i:Cerebrovasc Dis
Main Authors: Choquet, Hélène, Pawlikowska, Ludmila, Nelson, Jeffrey, McCulloch, Charles E., Akers, Amy, Baca, Beth, Khan, Yasir, Hart, Blaine, Morrison, Leslie, Kim, Helen
Format: Artigo
Sprog:Inglês
Udgivet: 2014
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Article
Online adgang: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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