Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common hereditary subcortical vascular dementia. It is caused by mutations in NOTCH3 gene, which encodes a large transmembrane receptor Notch3. The key pathological finding is the accumul...

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Main Authors: Tikka, Saara, Mykkänen, Kati, Ruchoux, Marie-Magdeleine, Bergholm, Robert, Junna, Maija, Pöyhönen, Minna, Yki-Järvinen, Hannele, Joutel, Anne, Viitanen, Matti, Baumann, Marc, Kalimo, Hannu
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2668941/
https://ncbi.nlm.nih.gov/pubmed/19174371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awn364
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