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KIF1A Hereditary Spastic Paraparesis
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Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis.
Yaniv Erlich, S. Edvardson, E. Hodges, et al. (2011). Genome research. Cited 198 times.
https://doi.org/10.1101/gr.117143.110
