MeSH Browser

MeSH Supplementary: antithrombin III Arg197STOP
Unique ID: C094963
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C094963
Registry Numbers: 0
Heading Mapped to: *Antithrombin III
Frequency: 2
Note: Arg(197) codon replaced by stop codon TGA (R197X); one of two mutations responsible for hereditary type Ia antithrombin III deficiency
Source: Thromb Res 1995 May 1;78(3):251-4
Date of Entry: 1995/09/06
Revision Date: 1996/07/23

antithrombin III Arg197STOP MeSH Supplementary Concept Data 2025