Skip to main content
. 2013 Nov 29;76(4):545–548. doi: 10.1292/jvms.13-0156

Fig. 3.

Fig. 3.

A: Sequence analysis of the exon 11 amplicon from Case 2. The arrow indicates a point mutation (c.1676T>A). B: Exon 11 nucleotide and amino acid sequences from Case 2. The point mutation (c.1676T>A) and the corresponding amino acid substitution (p.Val559Asp) are underlined and shown by bold letters.