Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis

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Figure 1.
Figure 1.

Pedigree of the affected family. Sex of the nonaffected individuals was randomized to prevent identification of the family.

This Article

  1. Published in Advance April 12, 2011, doi: 10.1101/gr.117143.110 Genome Res. 21: 658-664

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