Novel ATL1 mutation in a Chinese family with hereditary spastic paraplegia: A case report and review of literature

doi:10.12998/wjcc.v7.i11.1358

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Jun 6, 2019 (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. Jun 6, 2019; 7(11): 1358-1366
Published online Jun 6, 2019. doi: 10.12998/wjcc.v7.i11.1358

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Figure 1 The pedigree of the SPG3A family. The patient is indicated with arrow (III:1) and the affected families are indicated by solid boxes (I:1 and II:2).

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