Fig. 3From: A novel COL4A5 splicing mutation causes alport syndrome in a Chinese familyFamily pedigree and confirmation of the variant of COL4A5. (A) The pedigree of the family. Filled symbols represent affected individuals (black: the 4298-8 G > A variant carriers). Arrow indicates the proband. (B) Identification of COLAA5 variant in the family through Sanger sequencing, the arrows represent sites of variantBack to article page