Crimella C et al. Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot–Marie–Tooth type 2. Clinical genetics. 2012; 82(2), 157-164. PMID: 21623771.
Faruq M et al. Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation. Clinical Genetics. 2019;96(3), 271-273. PMID: 31286494.
Nicolas A et al. Genome-wide analyses identify KIF5A as a novel ALS gene. Neuron. 2018; 97(6), 1268-1283. PMID: 29566793.