BioMed Research International / 2021 / Article / Fig 1

Research Article

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

Figure 1

Pedigree 1 of the Alport syndrome family. Black-filled symbols represent patients carrying the c.422_428del (p.Leu142Valfs11) deletion mutation. The proband is marked with a black arrow.