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. 2011 Sep 27;3:71–77. doi: 10.1007/8904_2011_62

Fig. 1.

Fig. 1

Determination of the two novel PEPD mutations in patient gDNA. (a) 1131delACG, causing the deletion of Asp378 in exon 13. (b) 1301delT, causing a frameshift in exon 14 and the creation of a premature stop codon. The arrows indicate the position of the mutations