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HARVARD Citation
Lambe, J. et al. (2018). CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype. Practical neurology. 18 (5), pp. 369-372. [Online].
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Lambe, J. et al. (2018). CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype. Practical neurology. 18 (5), pp. 369-372. [Online].