Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms (Stroke (2008) 39 (e195) DOI: 10.1161/STROKEAHA.108.522631);Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

Stroke

Volumn 40, Issue 1, 2009, Pages 71-76

  Worrall, Bradford B ^a,g   Foroud, Tatiana ^b   Brown, Robert D ^c   Connolly, E Sander ^d   Hornung, Richard W ^e   Huston, John ^c   Kleindorfer, Dawn ^f   Koller, Daniel L ^b   Lai, Dongbing ^b   Moomaw, Charles J ^f   Sauerbeck, Laura ^f   Woo, Daniel ^f   Broderick, Joseph P ^f  

^a UNIVERSITY OF VIRGINIA   (United States)

^b INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c MAYO CLINIC   (United States)

^d Columbia University ^*  (United States)

^e CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^f UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^g UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

Author keywords

Aortic aneurysms; Genetic linkage; Genetic susceptibility; Intracranial aneurysm; Single nucleotide polymorphism

Indexed keywords

ABDOMINAL AORTA; AORTA ANEURYSM; ARTICLE; CHROMOSOME 11; CHROMOSOME 6; CHROMOSOME ANALYSIS; CONTROLLED STUDY; FEMALE; GENETIC LINKAGE; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENOME ANALYSIS; HUMAN; INTRACRANIAL ANEURYSM; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD REVIEW; PHENOTYPE; PRIORITY JOURNAL; THORACIC AORTA; ADULT; AGED; CHROMOSOME MAP; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; INHERITANCE; METABOLISM; METHODOLOGY; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY;

ADULT; AGED; AORTIC ANEURYSM; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 6; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HUMANS; INHERITANCE PATTERNS; INTRACRANIAL ANEURYSM; MALE; MIDDLE AGED; MUTATION; PHENOTYPE;

EID: 60549092893     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/STROKEAHA.107.000011     Document Type: Erratum

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