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. 2017 Sep 26;17:173. doi: 10.1186/s12886-017-0567-3

Fig. 5.

Fig. 5

The c.8326G > A homozygous change of the VSX1 gene. The sequence of a normal control (a) included the nucleotide G at position 8326 in the third intron of VSX1. The variant sequence (b) showed a G to A homozygous transition (arrow), which results in a c.8326G > A SNP change