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A novel homozygous mutation in ATP13A2 gene causing pure hereditary spastic paraplegia
Rui Ban1, Chuanqiang Pu2, Fang Fang1
1Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, China.
Abstract:
SPG78 is a subtype of hereditary spastic paraplegia(HSP) caused by ATP13A2 gene mutations. SPG78 was reported as complicated HSP in several cases, but was never associated with pure HSP. Here we report the first Chinese patient carrying a novel homozygous nonsense mutation in ATP13A2 presenting with pure HSP.
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