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• W2153669677 abstract "Due to a homozygous Gly204Arg mutation in the factor X (FX) gene no detectable FX antigen was found in the plasma of a one-year old patient with severe bleeding diathesis. The amino acid replacement destabilized the disulfide bond that holds the two FX chains together, decreasing the interaction between the Cys201-Cys206 loop region and the region connecting the EGF2 and serine protease domains. Both Gly204 FX and Arg204 FX were synthesized in transfected cells, but only the wild type protein became secreted. The mutant protein was diverted from the normal secretory pathway and retained at the trans Golgi-late endosome level." @default.
• W2153669677 created "2016-06-24" @default.
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• W2153669677 date "2008-02-01" @default.
• W2153669677 modified "2023-10-16" @default.
• W2153669677 title "Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency" @default.
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• W2153669677 doi "https://doi.org/10.3324/haematol.11746" @default.
• W2153669677 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18245654" @default.
• W2153669677 hasPublicationYear "2008" @default.
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