From the syndrome of charcot, marie and tooth to disorders of peripheral myelin proteins

Brain

Volumn 118, Issue 3, 1995, Pages 809-818

  Harding, A E ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Charcot Marie Tooth disease; Connexin 32; Hereditary motor and sensory neuropathy; Hereditary neuropathy with liability to pressure palsies; P0; Peripheral myelin protein 22

Indexed keywords

GAP JUNCTION PROTEIN; MYELIN PROTEIN;

CHROMOSOME 17; DIAGNOSTIC ACCURACY; DISEASE CLASSIFICATION; DOMINANT INHERITANCE; FAMILY; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENETIC COUNSELING; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NERVE CONDUCTION; PARALYSIS; POINT MUTATION; PRIORITY JOURNAL; REVIEW;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOMES, HUMAN, PAIR 17; CONNEXINS; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; LINKAGE (GENETICS); MULTIGENE FAMILY; MYELIN P0 PROTEIN; MYELIN PROTEINS; NEURAL CONDUCTION; POINT MUTATION; PRESSURE; SEQUENCE DELETION; X CHROMOSOME;

EID: 0029058673     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/118.3.809     Document Type: Review

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