Association of neprilysin polymorphism with cerebral amyloid angiopathy
Association of neprilysin polymorphism with cerebral amyloid angiopathy
About this item
Full title
Author / Creator
Yamada, M , Sodeyama, N , Itoh, Y , Takahashi, A , Otomo, E , Matsushita, M and Mizusawa, H
Publisher
London: BMJ Publishing Group Ltd
Journal title
Language
English
Formats
Publication information
Publisher
London: BMJ Publishing Group Ltd
Subjects
More information
Scope and Contents
Contents
Objectives: The risk of sporadic cerebral amyloid angiopathy (CAA) may be associated with genetic polymorphisms of molecules related to anabolism or catabolism of amyloid β protein (Aβ). The authors investigated whether a polymorphism of the gene (NEP) coding for neprilysin, an enzyme catabolising Aβ, is associated with CAA. Methods: The study anal...
Alternative Titles
Full title
Association of neprilysin polymorphism with cerebral amyloid angiopathy
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1738486
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1738486
Other Identifiers
ISSN
0022-3050
E-ISSN
1468-330X
DOI
10.1136/jnnp.74.6.749
