Genetic heterogeneity in rapid onset dystonia-parkinsonism: Description of a new family

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 76, Issue 6, 2005, Pages 860-862

  Kabakci, K ^a   Isbruch, K ^b   Schilling, K ^c   Hedrich, K ^a   De Carvalho Aguiar, P ^d   Ozelius, L J ^d   Kramer, P L ^c   Schwarz, M H R M ^b   Klein, Christine ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b KLINIKUM DORTMUND   (Germany)

^c UNIVERSITY OF PORTLAND   (United States)

^d ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM) ALPHA3; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 19Q; CHROMOSOME 8; CLINICAL ARTICLE; DISEASE DURATION; DYSTONIA; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; MALE; MOTOR DYSFUNCTION; ONSET AGE; PARKINSONISM; PEDIGREE; PRIORITY JOURNAL; STATISTICAL ANALYSIS;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 19; DISEASE PROGRESSION; DYSTONIA; FEMALE; GENETIC HETEROGENEITY; HUMANS; MALE; MOLECULAR BIOLOGY; PARKINSON DISEASE; PEDIGREE;

EID: 20444416430     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.2004.046730     Document Type: Article

References (11)

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