Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Annals of Neurology

Volumn 42, Issue 6, 1997, Pages 924-932

  Schöls, Ludger ^a   Amoiridis, Georgios ^a   Büttner, Thomas ^a   Przuntek, Horst ^a   Epplen, Jörg T ^b   Riess, Olaf ^b  

^a ST JOSEF HOSPITAL   (Germany)

^b RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CEREBELLAR ATAXIA; CLINICAL FEATURE; DIPLOPIA; DISEASE SEVERITY; EVOKED MUSCLE RESPONSE; GENE MUTATION; GENETIC SUSCEPTIBILITY; HUMAN; HYPOREFLEXIA; MAJOR CLINICAL STUDY; MYOCLONUS; NUCLEOTIDE REPEAT; ONSET AGE; PATHOGENESIS; PRIORITY JOURNAL; TREMOR;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; CEREBELLAR ATAXIA; CHILD; EVOKED POTENTIALS, MOTOR; FEMALE; HUMANS; LINEAR MODELS; MALE; MIDDLE AGED; MUTATION; NEURAL CONDUCTION; PHENOTYPE; TRINUCLEOTIDE REPEATS;

EID: 2642589007     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420615     Document Type: Article

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