Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19p

Annals of Neurology

Volumn 41, Issue 1, 1997, Pages 8-16

  Baloh, Robert W ^a   Yue, Qing ^a   Furman, Joseph M ^b   Nelson, Stanley F ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 19P; CLINICAL ARTICLE; EYE MOVEMENT; FAMILIAL DISEASE; FEMALE; GENETIC LINKAGE; HEMIPLEGIA; HEREDITARY ATAXIA; HUMAN; MALE; MIGRAINE; NYSTAGMUS; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CEREBELLAR ATAXIA; CHROMOSOMES, HUMAN, PAIR 19; EYE MOVEMENTS; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; PEDIGREE;

EID: 0031015937     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410410105     Document Type: Article

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