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Q35161567-9D01F95D-6B0D-454E-9B2A-61E35BC14FCC
Q35161567-9D01F95D-6B0D-454E-9B2A-61E35BC14FCC
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Statement
http://www.wikidata.org/entity/statement/Q35161567-9D01F95D-6B0D-454E-9B2A-61E35BC14FCC
KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2.
P2860
Q35161567-9D01F95D-6B0D-454E-9B2A-61E35BC14FCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35161567-9D01F95D-6B0D-454E-9B2A-61E35BC14FCC
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wasDerivedFrom
45d1d2fceb5bee10b21e0f2d3567027a45428507
P2860
Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.