Human Genome Epidemiology Literature Finder
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Query Trace: Ataxia and SCA18[original query] |
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Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxia. Journal of human genetics 2018 1 63 (4): 521-524. Lin Pengfei, Zhang Dong, Xu Guangrun, Yan Chuanz |
- Page last reviewed:Feb 1, 2024
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