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Figure 1: Multiple alignments of HCV REFSEQ sequences against our sequence (HCV 4HZ). The 5`UTR region from our patient was cloned and sequenced using standard procedures as described in Materials and Methods. The 4a.Eg.HZ sequence was aligned against the HCV REFSEQ sequences using BIOEDIT program (Hall, 1998). Subdomain IIId here starts from nucleotide 280. Positions 281 and 282 are the locations of the detected dinucleotide mutation

Figure 1: Multiple alignments of HCV REFSEQ sequences against our sequence (HCV 4HZ). The 5`UTR region from our patient was cloned and sequenced using standard procedures as described in Materials and Methods. The 4a.Eg.HZ sequence was aligned against the HCV REFSEQ sequences using BIOEDIT program (Hall, 1998). Subdomain IIId here starts from nucleotide 280. Positions 281 and 282 are the locations of the detected dinucleotide mutation