CNKSR2 mutation causes the X-linked epilepsy-aphasia syndrome: A case report and review of literature

doi:10.12998/wjcc.v6.i12.570

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Oct 26, 2018 (publication date) through Nov 3, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Oct 26, 2018; 6(12): 570-576
Published online Oct 26, 2018. doi: 10.12998/wjcc.v6.i12.570

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Figure 4 Tertiary structures of wild-type and mutated CNKSR2 proteins predicted by RaptorX. The spatial structures of CNKSR2 proteins are significantly different between the wild-type (A) and the patient (B).

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