Skip to main content
. 2001 Dec;159(6):2017–2022. doi: 10.1016/S0002-9440(10)63053-2

Figure 4.

Figure 4.

Non-sense mutation of the STK11/LKB1 gene (exon 2) in the PJS-associated IPMN (case 2). The arrow indicates a single nucleotide change from C to T, resulting in a premature stop codon at 123. The corresponding sequence in case 15 (sporadic IPMN) is wild type.