Whole-Exome Sequencing Reveals a Rare Missense Variant in <i>SLC16A9</i> in a Pedigree with Early-Onset Gout

<div>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&gt;A (p.L93M).</div>

BioMed Research International

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Figure 1: Whole-Exome Sequencing Reveals a Rare Missense Variant in <i>SLC16A9</i> in a Pedigree with Early-Onset Gout 

BioMed Research International

Whole-Exome Sequencing Reveals a Rare Missense Variant in SLC16A9 in a Pedigree with Early-Onset Gout

Figure 1