Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification

Journal of Neurology

Volumn 258, Issue 9, 2011, Pages 1637-1642

  Kostić, Vladimir S ^a   Lukić Ječmenica, Milica ^a   Novaković, Ivana ^a   Dobričić, Valerija ^a   Brajković, Lela ^b   Krajinović, Maja ^c   Klein, Christine ^d   Pavlović, Aleksandra ^a  

^a UNIVERSITY OF BELGRADE   (Serbia)

^b CLINICAL CENTER OF SERBIA   (Serbia)

^c UNIVERSITY OF MONTREAL   (Canada)

^d UNIVERSITY OF LÜBECK   (Germany)

Author keywords

Genetic heterogeneity; Idiopathic basal ganglia calcification

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOME; BRAIN CALCIFICATION; CHROMOSOME 14Q; CHROMOSOME 2Q37; CHROMOSOME 8P21.1; CHROMOSOME 8P21.1-Q11.23; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; DYSKINESIA; FEMALE; FRONTAL CORTEX; GAIT DISORDER; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC SCREENING; GENOTYPE; HAMILTON SCALE; HUMAN; IDIOPATHIC BASAL GANGLIA CALCIFICATION; LINKAGE ANALYSIS; MALE; MINI MENTAL STATE EXAMINATION; ONSET AGE; PARKINSONISM; PRIORITY JOURNAL; SERBIA; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY;

ADULT; AGED; AGED, 80 AND OVER; BASAL GANGLIA DISEASES; CALCINOSIS; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; PEDIGREE; SERBIA;

EID: 80052968906     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-011-5985-1     Document Type: Article

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