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Figure 2: The nucleotide sequence of the Exon 3 in the APRT allele showing a homozygous point mutation at codon 200 CGA to CAA (NM_000485.2:c. 200G>A)

Figure 2: The nucleotide sequence of the Exon 3 in the APRT allele showing a homozygous point mutation at codon 200 CGA to CAA (NM_000485.2:c. 200G>A)