KLC2
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Kinesin light chain 2 is a protein that in humans is encoded by the KLC2 gene. This gene is responsible for SPOAN syndrome, a type of hereditary spastic paraplegia.
Kinesin light chain 2 is a protein that in humans is encoded by the KLC2 gene. This gene is responsible for SPOAN syndrome, a type of hereditary spastic paraplegia.
Text derived from https://en.wikipedia.org/w/index.php?oldid=1373836641 under CC BY-SA 4.0; modifications have been made.