Whole Exome Sequencing Identifies Two Novel Mutations in a Patient with UC Associated with PSC and SSA

<div>(a) Liver biopsy revealing portal infiltration of lymphocytes, plasmacytes, and scattered eosinophils with fibrosis and pseudolobule (H&amp;E, 10 × 10). (b) Histological examination demonstrating neutrophilic microabscesses in the crypts (H&amp;E, 10 × 20).</div>

Canadian Journal of Gastroenterology and Hepatology

fig4

Figure 4

Figure 4: Whole Exome Sequencing Identifies Two Novel Mutations in a Patient with UC Associated with PSC and SSA 