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Comprehensive mutation scanning of KCNQ1 in 111 Han Chinese patients with lone atrial fibrillation
OBJECTIVE: To determine the extent to which genetic variation in the potassium channel gene KCNQ1 causes atrial fibrillation (AF). DESIGN: Case–control study. SETTING: National University Hospital, Singapore. PATIENTS: Han Chinese patients (n=111) with lone AF (onset <60 years and lacking risk fa...
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| 發表在: | Heart Asia |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BMJ Publishing Group
2010
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4898533/ https://ncbi.nlm.nih.gov/pubmed/27325960 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ha.2010.002832 |
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