Overview of Charcot-Marie-Tooth disease type 1A

Annals of the New York Academy of Sciences

Volumn 883, Issue , 1999, Pages 1-5

  Thomas, P K ^a,b  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALLIUM CEPA; ATAXIA;

MYELIN PROTEIN; PMP22 PROTEIN, HUMAN;

CHROMOSOME 17; CLASSIFICATION; GENE DUPLICATION; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; PATHOPHYSIOLOGY; POINT MUTATION; PRESCHOOL CHILD; REVIEW;

CHARCOT-MARIE-TOOTH DISEASE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; GENE DUPLICATION; HUMANS; MYELIN PROTEINS; POINT MUTATION;

EID: 0033554351     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb08560.x     Document Type: Article

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