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- W2390678249 abstract "Objective To study gene defect of a hereditary coagulation factor XIII deficiency family.Methods PCR and gene sequencing were used to detect the FXIIIA gene of peripheral white blood cell from a hereditary coagulation factor XIII deficiency family members.Results The proband had a del-aa at nucleotide(nt) 72045 in exon 5,both of her parents and sister were correspondingly heterozygotes at the same nucleotide.Conclusion The mutation was resulted in FXIIIA deficiency." @default.
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- W2390678249 date "2007-01-01" @default.
- W2390678249 modified "2023-09-26" @default.
- W2390678249 title "Gene mutation detection for hereditary coagulation factor XIII deficiency" @default.
- W2390678249 hasPublicationYear "2007" @default.
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