Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites

Neurology

Volumn 78, Issue 9, 2012, Pages 649-657

  Saunders Pullman, R ^a,b   Raymond, D ^a   Stoessl, A J ^c   Hobson, D ^d   Nakamura, T ^e   Pullman, S ^f   Lefton, D ^b   Okun, M S ^g   Uitti, R ^h   Sachdev, R ^k   Stanley, K ^a   San Luciano, M ^a   Hagenah, J ⁱ   Gatti, R ^e   Ozelius, L J ^j   Bressman, S B ^a,b  

^a BETH ISRAEL MEDICAL CENTER   (United States)

^b ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^d UNIVERSITY OF MANITOBA   (Canada)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f Och Spine at New York Presbyterian Hospitals   (United States)

^g UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^h MAYO CLINIC   (United States)

ⁱ UNIVERSITY OF LÜBECK   (Germany)

^j MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^k NONE

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATAXIA TELANGIECTASIA; CANADA; CEREBELLUM ATROPHY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DYSTONIA; ETHNIC GROUP; FEMALE; FOUNDER EFFECT; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; HOMOZYGOSITY; HUMAN; MALE; MALIGNANT NEOPLASTIC DISEASE; MYOCLONUS DYSTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; RELATIVE;

EID: 84863267494     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3182494d51     Document Type: Article

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