Electrodiagnostic studies in a murine model of demyelinating Charcot-Marie-Tooth disease

Physical Medicine and Rehabilitation Clinics of North America

Volumn 16, Issue 4, 2005, Pages 967-979

  Meekins, Gregg D ^a   Weiss, Michael D ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PERIPHERAL MYELIN PROTEIN 22;

AMINO ACID SUBSTITUTION; DEMYELINATION; ELECTRODIAGNOSIS; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; HEREDITARY MOTOR SENSORY NEUROPATHY; INNERVATION; MOTOR UNIT; MUSCLE ATROPHY; MUSCLE WEAKNESS; NERVE CONDUCTION; NEUROMUSCULAR SYNAPSE; NONHUMAN; PATHOPHYSIOLOGY; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; REVIEW; TREMOR;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; DISEASE MODELS, ANIMAL; ELECTROMYOGRAPHY; HUMANS; MICE; MUSCLE FIBERS; MUTATION; NEURAL CONDUCTION; PHENOTYPE;

EID: 26244441315     PISSN: 10479651     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pmr.2005.08.006     Document Type: Review

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