Common genetic polymorphisms in Moyamoya and atherosclerotic disease in Europeans

Child's Nervous System

Volumn 27, Issue 2, 2011, Pages 245-252

  Roder, Constantin ^a   Peters, Vera ^a   Kasuya, Hidetoshi ^b   Nishizawa, Tsutomu ^c   Takehara, Yayoi ^c   Berg, Daniela ^d   Schulte, Claudia ^e   Khan, Nadia ^f   Tatagiba, Marcos ^a   Krischek, Boris ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^c TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^d GERMAN CENTER FOR NEURODEGENERATIVE DISEASES DZNE   (Germany)

^e UNIVERSITY OF TÜBINGEN   (Germany)

^f STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Atherosclerotic disease; Genetics; Moyamoya disease; Single nucleotide polymorphism

Indexed keywords

CADHERIN; CYCLIN DEPENDENT KINASE INHIBITOR 2A; CYCLIN DEPENDENT KINASE INHIBITOR 2B; DNA; ELASTIN; LIM KINASE 1; PLATELET DERIVED GROWTH FACTOR B; SMAD3 PROTEIN; STROMAL CELL DERIVED FACTOR 1;

3' UNTRANSLATED REGION; ADULT; ARTICLE; ATHEROSCLEROSIS; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; FEMALE; GENE; GENE FREQUENCY; GENE LOCATION; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; GERMANY; HUMAN; MALE; MOYAMOYA DISEASE; ONSET AGE; PRIORITY JOURNAL; PROLINE SERINE RICH COILED COIL 1 GENE; QUESTIONNAIRE; SINGLE NUCLEOTIDE POLYMORPHISM; SWITZERLAND;

EID: 78951477995     PISSN: 02567040     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00381-010-1241-8     Document Type: Article

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