Degenerative myelopathy associated with a missense mutation in the superoxide dismutase 1 (SOD1) gene progresses to peripheral neuropathy in Pembroke Welsh Corgis and Boxers

Journal of the Neurological Sciences

Volumn 318, Issue 1-2, 2012, Pages 55-64

  Shelton, G Diane ^a   Johnson, Gayle C ^b   O'Brien, Dennis P ^b   Katz, Martin L ^b   Pesayco, Jill P ^a   Chang, Brian J ^a   Mizisin, Andrew P ^a   Coates, Joan R ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF MISSOURI   (United States)

Author keywords

Amyotrophic lateral sclerosis; Animal model; Axonopathy; Axons; Canine; Dog; Neuropathy; Schwann cells

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; DEGENERATIVE MYELOPATHY; DEMYELINATION; DISEASE COURSE; HISTOPATHOLOGY; MISSENSE MUTATION; MUSCLE ATROPHY; MUSCLE DENERVATION; NERVE FIBER DEGENERATION; NONHUMAN; PERIPHERAL NERVE; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SPINAL CORD DISEASE;

ANIMALS; DISEASE MODELS, ANIMAL; DISEASE PROGRESSION; DOG DISEASES; DOGS; GENETIC PREDISPOSITION TO DISEASE; HEREDODEGENERATIVE DISORDERS, NERVOUS SYSTEM; HOMOZYGOTE; MUTATION, MISSENSE; PERIPHERAL NERVOUS SYSTEM DISEASES; SPINAL CORD DISEASES; SUPEROXIDE DISMUTASE;

EID: 84861648435     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2012.04.003     Document Type: Article

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