Role of kinesin-1 in the pathogenesis of SPG10, a rare form of hereditary spastic paraplegia

Neuroscientist

Volumn 19, Issue 4, 2013, Pages 336-344

  Kawaguchi, Kenji ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

axon neurodegeneration; hereditary spastic paraplegia; KIF5A; kinesin 1; SPG10

Indexed keywords

KINESIN 1;

ARTICLE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MITOCHONDRION; NERVE FIBER; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN STRUCTURE; SPASTIC PARAPLEGIA TYPE 10;

AXON NEURODEGENERATION; HEREDITARY SPASTIC PARAPLEGIA; KIF5A; KINESIN-1; SPG10;

ANIMALS; HUMANS; KINESIN; MICE; MICE, KNOCKOUT; MICROTUBULES; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 84879993265     PISSN: 10738584     EISSN: 10894098     Source Type: Journal    
DOI: 10.1177/1073858412451655     Document Type: Article

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