Skip to main content
. 2021 Jul 7;108(8):1466–1477. doi: 10.1016/j.ajhg.2021.06.010

Figure 1.

Figure 1

Identification of bi-allelic DNAH10 variants in men with asthenoteratozoospermia

(A) Pedigrees of four families affected by DNAH10 variants (M1–M6) identified via WES. Male individuals with asthenoteratozoospermia in these families are indicated by black-filled squares. The double lines indicate first-degree consanguinity.

(B) Sanger sequencing confirmed the presence of bi-allelic DNAH10 variants (M1–M6) in T012 II-2, T089 II-1, H049 II-2, NK067 II-1, and NK067 II-2. The variant positions are indicated by using red arrows. WT, wild-type.