MeSH Browser

MeSH Supplementary: fibrinogen Nieuwegein
Unique ID: C422763
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C422763
Registry Number: 0
Heading Mapped to: *Fibrinogens, Abnormal
Frequency: 2
Note: has a homozygous insertion of a single nucleotide (C) in codon Aalpha 453 (Pro) which introduced a stop codon at position 454 resulting in the deletion of the carboxyl-terminal segment Aalpha 454-610
Source: Blood 2001 Feb 15;97(4):973-80
Date of Entry: 2001/03/28

fibrinogen Nieuwegein MeSH Supplementary Concept Data 2024