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HARVARD Citation
Helbig, K. et al. (n.d.). A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Annals of neurology. 80 (4), p. n/a. [Online].
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Helbig, K. et al. (n.d.). A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Annals of neurology. 80 (4), p. n/a. [Online].