Rapid-onset dystonia-parkinsonism: A fourth family consistent with linkage to chromosome 19q13

Movement Disorders

Volumn 19, Issue 12, 2004, Pages 1506-1510

  Zaremba, Jacek ^a   Mierzewska, Hanna ^a   Lysiak, Zofia ^a   Kramer, Patricia ^b   Ozelius, Laurie J ^c   Brashear, Allison ^d  

^a INSTITUTE OF PSYCHIATRY AND NEUROLOGY   (Poland)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Dystonia; DYT12; Parkinsonism; RDP

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 19Q; CHROMOSOME MARKER; CLINICAL FEATURE; DIAGNOSTIC ERROR; EUROPE; FEMALE; GENETIC LINKAGE; HAPLOTYPE; HUMAN; MALE; MOTOR DYSFUNCTION; NUCLEOTIDE SEQUENCE; POLAND; PRIORITY JOURNAL; RAPID ONSET DYSTONIA PARKINSONISM;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CHROMOSOMES, HUMAN, PAIR 19; DYSTONIA; FEMALE; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; PARKINSONIAN DISORDERS; PEDIGREE;

EID: 3242694390     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.20258     Document Type: Article

References (8)

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8. Kamm C, Leung J, Joseph S, Dobyns WB, Brashear A, Breakefield XO, Ozelius LJ. Refined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene. Mov Disord 2004;19:845-847.