Genotype correlation with fine motor symptoms in patients with Wilson's disease

European Neurology

Volumn 48, Issue 2, 2002, Pages 97-101

  Hermann, Wieland ^a   Caca, Karel ^a   Eggers, Birk ^a   Villmann, Thomas ^a   Clark, Daniel ^a   Berr, Frieder ^a   Wagner, Armin ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

Fine motor functions; Genotype phenotype; H1069Q; Handwriting test; Wilson's disease

Indexed keywords

ADULT; ARTICLE; BASAL GANGLION; CEREBELLUM; CLINICAL ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE COURSE; DISEASE SEVERITY; FEMALE; GENE MUTATION; GENOTYPE; HANDWRITING; HUMAN; MALE; NEUROPATHOLOGY; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ADULT; CATION TRANSPORT PROTEINS; FEMALE; GENOTYPE; HANDWRITING; HEPATOLENTICULAR DEGENERATION; HUMANS; MALE; MIDDLE AGED; MOTOR SKILLS; MUTATION; PHENOTYPE;

EID: 0036373594     PISSN: 00143022     EISSN: None     Source Type: Journal    
DOI: 10.1159/000062992     Document Type: Article

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