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. 2008 Oct 1;17(3):344–351. doi: 10.1038/ejhg.2008.175

Figure 1.

Figure 1

Heterozygous mutations detected in ASD patients. (a) A change G:G/T at position 779 detected in patient no. 17 from group 2 with ASD, aneurysm of interatrial septum and other defects. (b) A change A:A/C at position 122 433 (1191 in cDNA) detected in patient no. 10 from group 1 with ASD symptoms alone. In the presented case, the sequence was obtained with the use of reverse primer to sequence the fragment starting at the position 121 553 (exons 4 and 5). (c) A change T:C at position 130 814 (1360 in cDNA) detected in the patient no. 1 from group 2 with ASD, aneurysm of intersinal septum and other defects. (d) A change A:A/G at position 187 409 (1885 in cDNA) detected in the patient no. 9 from group 2 with ASD, aneurysm of intersinal septum and other defects. Arrow in each panel indicates the detected changes.