Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from Northern Germany

Annals of Human Genetics

Volumn 63, Issue 4, 1999, Pages 285-291

  Klein, C ^a   Vieregge, P ^b   Hagenah, J ^c   Sieberer, M ^d   Doyle, E ^e   Jacobs, H ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b UNIVERSITY OF LÜBECK   (Germany)

^c LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^d STANFORD UNIVERSITY   (United States)

^e Molecular Genetics   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; ALPHA SYNUCLEIN; PROLINE;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 2P; COHORT ANALYSIS; CONTROLLED STUDY; ETHNIC GROUP; FEMALE; FOUNDER EFFECT; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GERMANY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEIC ACID BASE SUBSTITUTION; PARKINSON DISEASE; PRIORITY JOURNAL;

AGED; AGED, 80 AND OVER; ALLELES; ALPHA-SYNUCLEIN; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 2; COHORT STUDIES; FEMALE; FOUNDER EFFECT; GENE FREQUENCY; GENES, DOMINANT; GERMANY; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; NERVE TISSUE PROTEINS; PARKINSON DISEASE; POINT MUTATION; SYNUCLEINS;

EID: 0033376955     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480099007551     Document Type: Article

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