BioMed Research International / 2021 / Article / Fig 2

Research Article

Novel Mutations of COL4A5 Identified in Chinese Families with X-Linked Alport Syndrome and Literature Review

Figure 2

Pedigree 2 of the Alport syndrome family. Black-filled symbols represent patients carrying the c.476G>T (p.Gly159Val) missense mutation. The proband is marked with a black arrow.