Hereditary demyelinating neuropathies: From gene to disease

Neurogenetics

Volumn 3, Issue 2, 2001, Pages 53-57

  Hanemann, C O ^a  

^a UNIVERSITY OF ULM   (Germany)

Author keywords

Charcot Marie Tooth disease; Genotype; Hereditary demyelinating neuropathies; Pathogenesis; Phenotype

Indexed keywords

MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

ANIMAL; DEMYELINATING DISEASE; GENETICS; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUTATION; PATHOLOGY; PHENOTYPE; REVIEW;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; DEMYELINATING DISEASES; GENOTYPE; HUMANS; MUTATION; MYELIN PROTEINS; PHENOTYPE;

EID: 0035290467     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100480000102     Document Type: Review

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