Skip to main content
. 2017 Nov 9;9(1):122–141. doi: 10.18632/oncotarget.22343

Figure 2. Sequencing results of the (c.T734C:p.L245P) PROM1 mutation.

Figure 2

A. The novel heterozygous missense mutation (PROM1: NM_006017: exon7: c.T734C:p.L245P) of PROM1 gene in proband (II:2). B. Sanger sequencing results of IV:2 identified as a wild type. C. The wild type IV:1 was validated in the unaffected family individuals and unrelated normal controls, with the normal male from no eye disease history family (III:1). All number were depicted in Figure 1. The arrows indicate the mutation at the nucleotide position c. 734T > C in the PROM1 gene.