Figure 3
From: Significance of somatic mutations and content alteration of mitochondrial DNA in esophageal cancer

Alignment of novel germline missense mutations A: Case E02, A11976C (Y406S in ND4) and B: Case E16, G7921C (E109D in COII)
From: Significance of somatic mutations and content alteration of mitochondrial DNA in esophageal cancer
Alignment of novel germline missense mutations A: Case E02, A11976C (Y406S in ND4) and B: Case E16, G7921C (E109D in COII)