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Rare Coding Variation and Risk of Intracerebral Hemorrhage
BACKGROUND AND PURPOSE: Intracerebral hemorrhage (ICH) has a substantial genetic component. We performed a preliminary search for rare coding variants associated with ICH. METHODS: 757 cases and 795 controls were genotyped using the Illumina HumanExome Beadchip (Illumina, Inc. San Diego, CA, USA). M...
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| Pubblicato in: | Stroke |
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| Autori principali: | , , , , , , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4519408/ https://ncbi.nlm.nih.gov/pubmed/26111891 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/STROKEAHA.115.009838 |
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