Table 1.
Patient | Sex | CFTR mutation | T allele | TG repeats | PSTI mutation |
1 | M | ΔF508/R117H | 7/7 | 9/10 | –/– |
2 | W | ΔF508/A1087P | 7/9 | 10/11 | –/– |
3 | M | ΔF508/D1152H | 7/9 | 10/10 | –/– |
4 | M | S1235R/R668C | 7/7 | 11/12 | –/– |
5 | M | 2184insA/- | 7/7 | 10/12 | –/– |
6 | M | R31C/- | 7/7 | 10/11 | –/– |
7 | M | R75Q/- | 7/7 | 11/11 | –/– |
8 | M | R347P/- | 7/7 | 11/12 | –/– |
9 | M | S1235R/- | 7/7 | 11/12 | –/– |
10 | W | S1235R/- | 7/7 | 11/12 | –/– |
11 | M | G576A/- | 7/7 | 10/10 | –/– |
12 | W | M348V/- | 7/9 | 10/10 | –/– |
13 | M | V754M/- | 7/7 | 10/11 | –/– |
14 | M | –/– | 5/7 | 11/12 | –/– |
15 | W | –/– | 5/7 | 11/12 | –/– |
16 | M | –/– | 5/7 | 11/12 | –/– |
17 | W | –/– | 5/9 | 11/12 | –/– |
18 | M | –/– | 5/7 | 11/12 | –/– |
19 | M | –/– | 5/7 | 10/10 | –/– |
20 | W | –/– | 5/7 | 10/10 | –/– |
21 | W | –/– | 5/7 | 11/12 | N34S/- |
22 | W | –/– | 7/7 | 10/11 | N34S/- |
23 | M | –/– | 7/9 | 10/11 | N34S/- |
24 | M | –/– | 7/7 | 11/11 | N34S/- |
25 | M | –/– | 7/7 | 11/11 | N34S/- |
26 | W | –/– | 7/7 | 11/11 | N34S/- |
27 | M | –/– | 7/7 | 11/11 | N34S/- |
28 | W | –/– | 7/7 | 10/11 | N34S/- |
29 | W | –/– | 7/7 | 11/11 | P55S/- |
30 | W | –/– | 7/7 | 11/11 | IVS3+2TC/- |