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 2 Gene sequences of three members in the family.
A: De novo mutation of the CNKSR2 gene (c. 2185C>T, p.Arg729Ter) in the patient; B, C: No mutation was observed at the same locus in the parents (arrows).
- 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