Prevalence of FMR1 repeat expansions in movement disorders: A systematic review

Neuroepidemiology

Volumn 26, Issue 3, 2006, Pages 151-155

  Hall, D A ^a,e   Hagerman, R J ^b   Hagerman, P J ^c   Jacquemont, S ^d   Leehey, M A ^a  

^a UNIVERSITY OF COLORADO   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d NANTES UNIVERSITY HOSPITAL   (France)

^e UNIVERSITY OF COLORADO   (United States)

Author keywords

Cerebellar ataxia; Fragile X syndrome; Fragile X associated tremor ataxia syndrome; Parkinsonism

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN;

ADULT; ARTICLE; ATAXIA; COCHRANE LIBRARY; CONTROLLED STUDY; DATA BASE; EPIDEMIOLOGICAL DATA; ESSENTIAL TREMOR; FEMALE; FRIEDREICH ATAXIA; GENETIC SCREENING; GROUPS BY AGE; HUMAN; HUNTINGTON CHOREA; INFORMATION RETRIEVAL; MAJOR CLINICAL STUDY; MALE; MEDLINE; METHODOLOGY; MOTOR DYSFUNCTION; NUCLEOTIDE REPEAT; PARKINSONISM; POPULATION STRUCTURE; PREVALENCE; SHY DRAGER SYNDROME; SPINOCEREBELLAR DEGENERATION;

CROSS-SECTIONAL STUDIES; DNA REPEAT EXPANSION; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; HUMANS; MALE; MIDDLE AGED; MOVEMENT DISORDERS;

EID: 33645696348     PISSN: 02515350     EISSN: None     Source Type: Journal    
DOI: 10.1159/000091656     Document Type: Article

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