Dejerine-Sottas disease (progressive hypertrophic polyneuropathy)

European Neurology

Volumn 55, Issue 2, 2006, Pages 115-117

  Pearce, J M S ^a,b  

^a HULL ROYAL INFIRMARY   (United Kingdom)

^b NONE   (United Kingdom)

Author keywords

Dejerine Sottas disease; Hereditary motor and sensory neuropathy; Myelin proteins; Neurology and art

Indexed keywords

MYELIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; DEMYELINATION; DISEASE COURSE; DISEASE SEVERITY; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUSCLE ATROPHY; ONSET AGE; PRIORITY JOURNAL; WALKING DIFFICULTY; WEAKNESS;

FRANCE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HISTORY, 19TH CENTURY; HISTORY, 20TH CENTURY; HUMANS; SWITZERLAND;

EID: 33646809773     PISSN: 00143022     EISSN: None     Source Type: Journal    
DOI: 10.1159/000092790     Document Type: Article

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