Skip to main content
. 2024 Feb 15;14:1267967. doi: 10.3389/fendo.2023.1267967

Figure 1.

Figure 1

Pedigree, missense mutations and clinical manifestations of HSD17B3 deficiency patients. (A) Genitalia appearances of patients at first visit and following-up. (B) Family pedigree. Unavailable information of deceased father of Patient 2. (C) HSD17B3 DNA sequencing of the patients; the mutation site in HSD17B3 is marked with an arrow.