Copyright
©The Author(s) 2018.
World J Clin Cases. Oct 26, 2018; 6(12): 570-576
Published online Oct 26, 2018. doi: 10.12998/wjcc.v6.i12.570
Published online Oct 26, 2018. doi: 10.12998/wjcc.v6.i12.570
Figure 3 Secondary structures of wild-type and mutated CNKSR2 proteins predicted by PSIPRED.
A: The wild-type CNKSR2 gene encodes an intact peptide chain of 1034 amino acids; B: The mutated CNKSR2 gene leads to an early termination of the synthesis of the peptide chain and only No.1-728 amino acids are expressed.
- Citation: Sun Y, Liu YD, Xu ZF, Kong QX, Wang YL. CNKSR2 mutation causes the X-linked epilepsy-aphasia syndrome: A case report and review of literature. World J Clin Cases 2018; 6(12): 570-576
- URL: https://www.wjgnet.com/2307-8960/full/v6/i12/570.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v6.i12.570