F8CCoagulation Factor VIIIc Gene
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References in periodicals archive ?
Long distance PCR in detection of inversion mutations of F8C gene in hemophilia A patients.
High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype phenotype correlation.
In fact, unlike other frequent genetic disorders, such as hemophilia A, in which ~50% of patients carry an inversion of F8C intron 8 (1), and cystic fibrosis, in which the microdeletion DF508 is present in up to 80% of mutated alleles (16), no predominant or ethnicity-specific mutations were present in the FIX gene in patients with HB.