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. 2011 Oct;22(10):1815–1820. doi: 10.1681/ASN.2011040337

Figure 2.

Figure 2.

The novel single-base homozygous deletion (c.8355delA) in exon 53 of the cubilin (CUBN) gene that causes nephrotic syndrome in family A2410. Note that the sequence shown depicts the plus strand of chromosome 10 and that CUBN is encoded on the reverse strand, therefore showing a deletion of a T (thymine) rather than A (adenine).