Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication

Canadian Journal of Neurological Sciences

Volumn 26, Issue 3, 1999, Pages 196-200

  Dupré, Nicolas ^b   Bouchard, Jean Pierre ^b   Cossette, Louise ^b   Brunet, Denis ^b   Vanasse, Michel ^b   Lemieux, Bernard ^b   Mathon, Gilles ^b   Puymirat, Jack ^a  

^a LAVAL UNIVERSITY   (Canada)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ACTION POTENTIAL; ADOLESCENT; ADULT; ALLELE; ARTICLE; CANADA; CHILD; CHROMOSOME 17P; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; ELECTROPHYSIOLOGY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOTOR NERVE CONDUCTION; PHENOTYPE; PRIORITY JOURNAL; SOUTHERN BLOTTING;

EID: 0032769350     PISSN: 03171671     EISSN: None     Source Type: Journal    
DOI: 10.1017/S031716710000024X     Document Type: Article

References (24)

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