BioMed Research International / 2021 / Article / Fig 4

Research Article

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

Figure 4

(a) Sequence of the hemizygous c.422_428del variant (III-3, III-4). (b) Sequence of the heterozygous c.422_428del variant (I-2, II-12, and III-6). (c) Sequence of unaffected individuals (II-9, II-14, III-7, and III-8).