Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage

Subarachnoid aneurysmal hemorrhage (SAH) due to cerebral aneurysm rupture is a very serious disease resulting in high mortality rate. It has been known that genetic factors are involved in the risk of SAH. A recent breakthrough in genomic variation called copy number variation (CNV) has been reveale...

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Veröffentlicht in:	Journal of human genetics 2010-11, Vol.55 (11), p.726-730
Hauptverfasser:	Bae, Joon Seol, Cheong, Hyun Sub, Park, Byung Lae, Kim, Lyoung Hyo, Park, Tae Joon, Kim, Jason Yongha, Pasaje, Charisse Flerida A, Lee, Jin Sol, Cui, Tailin, Inoue, Ituro, Shin, Hyoung Doo
Format:	Artikel
Sprache:	eng
Schlagworte:	631/1647/2217/2138 631/208/726/649/2157 692/699/75/593/1370 Adult Age Aged Aged, 80 and over Aneurysm Asian Continental Ancestry Group - genetics Association analysis Biomedical and Life Sciences Biomedicine Copy number Databases, Genetic DNA Copy Number Variations - genetics Gene Dosage Gene Expression Gene Function Gene Therapy Genetic factors Genome, Human Genome-Wide Association Study - methods Genomes Genotype Genotypes Hemorrhage Human Genetics Humans Image processing Japan - epidemiology Middle Aged Molecular Medicine Oligonucleotide Array Sequence Analysis - methods original-article Polymorphism, Single Nucleotide - genetics Subarachnoid Hemorrhage - epidemiology Subarachnoid Hemorrhage - genetics
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