MeSH Browser

MeSH Supplementary: protein C London 1
Unique ID: C062234
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C062234
Registry Number: 0
Heading Mapped to: Protein C / *analogs & derivatives
Frequency: 1
Note: recurrent protein C mutation at Arg 169 (CGG replaced by TGG); causes thrombosis
Source: Nucleic Acids Res 1989;17(24):10513
Date of Entry: 1990/02/05
Revision Date: 1990/07/05

protein C London 1 MeSH Supplementary Concept Data 2024