Fig. 3
From: KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
Schematic representation of the KIF1A protein with all variants in the allelic disorders. All variants identified in spastic paraplegia are depicted above the schematic protein in red open triangles (autosomal dominant) or blue solid triangles (autosomal recessive), while variants in mental retardation type 9 and hereditary sensory neuropathy IIC are shown below the schematic in green open diamonds and purple solid dots, respectively. Protein domains are according to UniProt consortium (https://www.uniprot.org)
