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Association of neprilysin polymorphism with cerebral amyloid angiopathy
Objectives: The risk of sporadic cerebral amyloid angiopathy (CAA) may be associated with genetic polymorphisms of molecules related to anabolism or catabolism of amyloid ß protein (Aß). The authors investigated whether a polymorphism of the gene (NEP) coding for neprilysin, an enzyme catabolising A...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1738486/ https://ncbi.nlm.nih.gov/pubmed/12754344 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.74.6.749 |
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