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. 2020 Feb 10;16(7):1264–1273. doi: 10.7150/ijbs.38415

Figure 1.

Figure 1

Identification of SASH1 as the causative mutation in DUH in a Chinese family. (A) Pedigrees of members of a Chinese family with DUH. (B) Clinical features of the proband. (C) Mutation analysis identified c.1761C>G (p.Ser587Arg) in SASH1 in DUH.