Novel haplotypes in 17q21 are associated with progressive supranuclear palsy

Annals of Neurology

Volumn 56, Issue 2, 2004, Pages 249-258

  Pastor, Pau ^a   Ezquerra, Mario ^b   Perez, J Christian ^a   Chakraverty, Sumi ^a   Norton, Joanne ^a   Racette, Brad A ^a   McKeel, Dan ^a   Perlmutter, Joel S ^a   Tolosa, Eduardo ^b   Goate, Alison M ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b HOSPITAL CLÍNIC   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALLELE; ARTICLE; CHROMOSOME 17Q; CHROMOSOME 17Q21; CONTROLLED STUDY; CORTICOBASAL DEGENERATION; CRHR1 GENE; DEGENERATIVE DISEASE; GENE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; IMP5 GENE; MAJOR CLINICAL STUDY; MAPT GENE; NEUROFIBRILLARY TANGLE; NSF GENE; PATHOGENESIS; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; RISK ASSESSMENT; SAITOHIN GENE; SINGLE NUCLEOTIDE POLYMORPHISM; WTN3 GENE;

ADULT; AGED; BASAL GANGLIA; CASE-CONTROL STUDIES; CEREBRAL CORTEX; CHROMOSOMES, HUMAN, PAIR 17; DEMOGRAPHY; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; NEURODEGENERATIVE DISEASES; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK; SPAIN; SUPRANUCLEAR PALSY, PROGRESSIVE; TAU PROTEINS;

EID: 3843131833     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20178     Document Type: Article

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