BioMed Research International / 2021 / Article / Fig 5

Research Article

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

Figure 5

(a) Sequence of the hemizygous c.476G>T variant (III-10). (b) Sequence of the heterozygous c.476G>T variant (II-12).
(a)
(b)