Figure 2: Frequency and spectrum of specific base substitution mutations in mtDNA from WS patient and control liver.
From: Werner syndrome through the lens of tissue and tumour genomics

Frequency and spectrum of specific base substitution mutations as determined by Duplex Sequencing in mtDNA isolated from liver tissue of two WS patients (WS patients 1 and 2) and two control donors (Control donors 1 and 2).