Učitavanje...

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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: Yamada, M, Sodeyama, N, Itoh, Y, Takahashi, A, Otomo, E, Matsushita, M, Mizusawa, H
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2003
Teme:
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!