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. 2020 Jan 31;2020:4321419. doi: 10.1155/2020/4321419

Figure 1.

Figure 1

Identification of SLC16A9 missense in the family with early-onset gout. (a) Pedigree and cosegregation results. Affected individual is represented as a filled square. Normal individuals are shown as empty symbols. (b) Sanger sequencing confirmed the segregation of the rare missense variant, c.277C>A (p.L93M).