CMT with pyramidal features

Neurology

Volumn 60, Issue 4, 2003, Pages 696-699

  Vucic, S ^a   Kennerson, M ^a   Zhu, D ^a   Miedema, E ^a   Kok, C ^a   Nicholson, G A ^a,b  

^a UNIVERSITY OF SYDNEY   (Australia)

^b Department of Microbiology and Infectious Diseases   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MUSCLE ATROPHY; MUSCLE WEAKNESS; NEUROPATHY; PHENOTYPE; PRIORITY JOURNAL; PYRAMIDAL SIGN;

EID: 0037465465     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000048561.61921.71     Document Type: Article

References (10)

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