Copyright
©The Author(s) 2019.
World J Clin Cases. Jun 6, 2019; 7(11): 1358-1366
Published online Jun 6, 2019. doi: 10.12998/wjcc.v7.i11.1358
Published online Jun 6, 2019. doi: 10.12998/wjcc.v7.i11.1358
Figure 2 DNA sequencing identified a novel ATL1 c.
752A>G, p.Q251R mutation (top: sequence of the patients; bottom: sequence of healthy individuals).
- Citation: Xiao XW, Du J, Jiao B, Liao XX, Zhou L, Liu XX, Yuan ZH, Guo LN, Wang X, Shen L, Lin ZY. Novel ATL1 mutation in a Chinese family with hereditary spastic paraplegia: A case report and review of literature. World J Clin Cases 2019; 7(11): 1358-1366
- URL: https://www.wjgnet.com/2307-8960/full/v7/i11/1358.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v7.i11.1358