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fibrinogen Tottori II
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
fibrinogen Tottori II
Unique ID
C489711
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C489711
Registry Number
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
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fibrinogen Tottori II
Preferred
Concept UI
M0472467
Registry Number
0
Terms
fibrinogen Tottori II
Preferred Term
Term UI
T609227
Date
09/13/2004
LexicalTag
NON
ThesaurusID
NLM (2004)
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