Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: A longitudinal clinical and electrophysiologic study

Neurology

Volumn 50, Issue 4, 1998, Pages 1061-1067

  García, Antonio ^a   Combarros, Onofre ^a   Calleja, Jesús ^a   Berciano, José ^a  

^a HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHILDHOOD DISEASE; CHROMOSOME 17P; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CLINICAL RESEARCH; ELECTROPHYSIOLOGY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INFANT; INFANT DISEASE; LONGITUDINAL STUDY; MALE; MOTOR NERVE CONDUCTION; NEWBORN; PRIORITY JOURNAL; SENSORY NERVE CONDUCTION;

EID: 0031900413     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.4.1061     Document Type: Article

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