Cite
HARVARD Citation
Dor, T. et al. (2014). KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction. Journal of medical genetics. 51 (2), pp. 137-142. [Online].
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Dor, T. et al. (2014). KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction. Journal of medical genetics. 51 (2), pp. 137-142. [Online].