Clinical and pathological phenotype of the original family with Charcot- Marie-Tooth type 1B: A 20-year study

Annals of Neurology

Volumn 41, Issue 4, 1997, Pages 463-469

  Bird, Thomas D ^a,b   Kraft, George H ^b   Lipe, Hillary P ^a   Kenney, Kimbra L ^c   Sumi, S Mark ^b  

^a VETERANS AFFAIRS MEDICAL CENTER   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN PROTEIN;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 1; CLINICAL ARTICLE; FEMALE; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOTOR NERVE CONDUCTION; MUSCLE WEAKNESS; NERVE BIOPSY; ONSET AGE; POINT MUTATION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; AXONS; BIOPSY; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; FIBROSIS; HUMANS; MALE; MICROSCOPY, ELECTRON; MIDDLE AGED; MYELIN PROTEINS; NEURAL CONDUCTION; PEDIGREE; PHENOTYPE; SPINAL NERVE ROOTS; SURAL NERVE;

EID: 0030993366     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410410409     Document Type: Article

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