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Q35603247-8603D5E0-7AE9-4E68-A06A-CF1A55568E69
Q35603247-8603D5E0-7AE9-4E68-A06A-CF1A55568E69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35603247-8603D5E0-7AE9-4E68-A06A-CF1A55568E69
Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity
P2860
Q35603247-8603D5E0-7AE9-4E68-A06A-CF1A55568E69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35603247-8603D5E0-7AE9-4E68-A06A-CF1A55568E69
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wasDerivedFrom
1e38a481ac850c4ac2364783f289becadcec9eeb
P2860
KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2.