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Fig. 3 | BMC Medical Genomics

Fig. 3

From: A novel large intragenic DPYD deletion causing dihydropyrimidine dehydrogenase deficiency: a case report

Fig. 3

Characterization of the breakpoints of the DPYD deletion. A Schematic illustration of part of the DPYD transcript variant NM_000110.4. Exons are represented by rectangles and intervening introns by lines. Red arrows denote the position of the breakpoints. B Nucleotide sequence, upstream and downstream of each breakpoint. The deleted sequence is indicated in blue letters. C Sequencing electropherogram of the patient at the junction region

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