MeSH Browser

MeSH Supplementary: fibrinogen Tottori II
Unique ID: C489711
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C489711
Registry Numbers: 0
Heading Mapped to: *Fibrinogens, Abnormal
Frequency: 1
Note: congenital hypofibrinogenemia is caused by a nonsense mutation in the fibrinogen Bbeta chain gene mutation (TAT sequence for Bbeta 41Tyr to TAG sequence for a translation termination signal)
Source: J Thromb Haemost 2003 Nov;1(11):2356-9
Date of Entry: 2004/09/13
Revision Date: 2004/09/13

fibrinogen Tottori II MeSH Supplementary Concept Data 2025