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Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis
Erlich Y,
Edvardson S,
Hodges E,
Zenvirt S,
Thekkat P,
Shaag A,
Dor T,
Hannon GJ,
Elpeleg O

Genome Research
  21 (5): 658-664; May 2011   PMCID: PMC3083082

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