Genetic variant on chromosome 12p13 does not show association to ischemic stroke in 3 Swedish case-control studies

Stroke

Volumn 42, Issue 1, 2011, Pages 214-216

  Olsson, Sandra ^d   Melander, Olle ^c   Jood, Katarina ^d,e   Smith, J Gustav ^b,c,f   Lövkvist, Håkan ^a,b   Sjögren, Marketa ^c   Engström, Gunnar ^c   Norrving, Bo ^a,b   Lindgren, Arne ^a,b   Jern, Christina ^d  

^a LUND UNIVERSITY   (Sweden)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

^c LUND UNIVERSITY   (Sweden)

^d UNIVERSITY OF GOTHENBURG   (Sweden)

^e SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^f MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

Genetic association studies; Single nucleotide polymorphism; Stroke

Indexed keywords

ADULT; AGED; ARTICLE; BRAIN ISCHEMIA; CASE CONTROL STUDY; CHROMOSOME 12P; CHROMOSOME 12P13; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; SWEDEN;

AGED; AGED, 80 AND OVER; BRAIN ISCHEMIA; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; STROKE; SWEDEN;

EID: 79451468882     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/STROKEAHA.110.594010     Document Type: Article

References (7)

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