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

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

BioMed Research International

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Figure 2

Figure 2: Novel Mutations of <i>COL4A5</i> Identified in Chinese Families with X-Linked Alport Syndrome and Literature Review 

BioMed Research International

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

Figure 2