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• W1991973433 abstract "Summary. We investigated the molecular basis of a severe factor V (FV) deficiency in a Japanese female, and identified two distinct mutations in the FV gene, a novel cytosine insertion (1943insC) and a previously reported point mutation (A5279G). We expected the patient to be a compound heterozygote for those mutations, as a 1943insC, but not an A5279G, was found in the mother and a sibling. The 1943insC will cause a frame‐shift after 590 Gln, resulting in amino acid substitutions with two abnormal residues followed by a stop codon in the FV A2 domain (FS592X). The A5279G will cause an amino acid alteration in the FV A3 domain (Y1702C), which has been observed in several ethnic groups. We found that both mutant mRNAs were detected by reverse transcriptase polymerase chain reaction (RT‐PCR) in the patient's platelets, whereas no FV antigen and activity were detected in plasma. On the one hand, the RT‐PCR signal from the FS592X‐FV mutant mRNA was markedly reduced, suggesting that the RNA surveillance system would eliminate most of the abnormal FS592X‐FV transcripts with a premature termination. On the other hand, expression analyses revealed that only small amounts of Y1702C‐FV with a low specific activity were secreted, and that the FS592X‐FV was not detected in cultured media. These data indicated that both mutant FV molecules would be impaired, at least in part, during the post‐transcriptional process of protein synthesis and/or in secretion. Taken together, it seems to suggest that each gene mutation could be separately responsible for severe FV deficiency, while this phenotype is due to the in‐trans combination of the two defects." @default.
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• W1991973433 date "2006-02-13" @default.
• W1991973433 modified "2023-10-16" @default.
• W1991973433 title "A case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene" @default.
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• W1991973433 doi "https://doi.org/10.1111/j.1365-2516.2006.01206.x" @default.
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