Genome-wide scan for Parkinson's disease: The GenePD study

Neurology

Volumn 57, Issue 6, 2001, Pages 1124-1126

  DeStefano, A L ^a,b   Golbe, L I ^d   Mark, M H ^d   Lazzarini, A M ^d   Maher, N E ^a   Saint Hilaire, M ^a   Feldman, R G ^a   Guttman, M ⁿ   Watts, R L ^e   Suchowersky, O ^o   Lafontaine, A L ^o   Labelle, N ^o   Lew, M F ^f   Waters, C H ^f   Growdon, J H ^c   Singer, C ^g   Currie, L J ^h   Wooten, G F ^h   Vieregge, P ^l   Pramstaller, P P ^m   Klein, C ^l   Hubble, J P ⁱ   Stacy, M ^j   Montgomery, E ^k   MacDonald, M E ^c   Gusella, J F ^c   Myers, R H ^a   more..

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b BOSTON UNIVERSITY   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

^e EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^g UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^h UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

ⁱ OHIO STATE UNIVERSITY   (United States)

^j Barrow Clinic   (United States)

^k LERNER RESEARCH INSTITUTE   (United States)

^l UNIVERSITY OF LÜBECK   (Germany)

^m CENTRAL HOSPITAL OF BOLZANO   (Italy)

ⁿ UNIVERSITY OF TORONTO   (Canada)

^o UNIVERSITY OF CALGARY   (Canada)

more..

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE BETA MONOOXYGENASE;

AGED; ARTICLE; CHILD; CHROMOSOME 1; CHROMOSOME 10; CHROMOSOME 16; CHROMOSOME 9; CLINICAL ARTICLE; DYSTONIA; GENE LOCUS; GENETIC LINKAGE; GENETIC SCREENING; GENOME; HUMAN; MALE; PARKINSON DISEASE; PRIORITY JOURNAL;

EID: 0035949797     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.57.6.1124     Document Type: Article

References (10)

1. Genetic influence on the development of Parkinson's disease
2. Variability and validity of polymorphism association studies in Parkinson's disease
3. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
4. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinicopathological study of 100 cases
5. Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs
6. Parametric and nonparametric linkage analysis: A unified multipoint approach
7. A susceptibility locus for Parkinson's disease maps to chromosome 2p13
8. The ubiquitin pathway in Parkinson's disease
9. A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase locus
10. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein