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Genome screen in familial intracranial aneurysm
BACKGROUND: Individuals with 1st degree relatives harboring an intracranial aneurysm (IA) are at an increased risk of IA, suggesting genetic variation is an important risk factor. METHODS: Families with multiple members having ruptured or unruptured IA were recruited and all available medical record...
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| Autors principals: | , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2636777/ https://ncbi.nlm.nih.gov/pubmed/19144135 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-3 |
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