Three Novel Mutations in the NPHS1 Gene in Vietnamese Patients with Congenital Nephrotic Syndrome

Figure 3

Mutations of the NPHS1 gene were identified by sequencing in patient 3 and his parents. The pedigree and mutations of the NPHS1 gene were identified in the family of patient 3, including of a homozygous variant p.Glu117Lys, a heterozygous mutation p.Lys792, and a heterozygous mutation p.Arg802Leu.