Fig. 2
From: Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated families
Family 2 pedigree. The proband is indicated with an arrow head
Fig. 2 | Human Genome Variation
From: Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated families
Family 2 pedigree. The proband is indicated with an arrow head
