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Heritability and genetics of atrial fibrillation
被引:1
|作者:
Aleong R.G.
[1
]
MacRae C.A.
[1
]
Ellinor P.T.
[1
]
机构:
[1] Massachusetts General Hospital, Boston, MA, 02114, 55 Fruit Street
关键词:
Atrial Fibrillation;
Lone Atrial Fibrillation;
KCNQ1 Mutation;
D O I:
10.1007/s12170-007-0068-7
中图分类号:
学科分类号:
摘要:
In the past 5 years, it has become increasingly clear that atrial fibrillation (AF) is a heritable condition. Mutations in six different ion channels have been described in families and individuals with AF, although screening of patients with AF reveals that these gene mutations appear to account for only rare cases of the disease. Recently, a genome-wide association study has identified a novel region of susceptibility for AF on chromosome 4. Our hope is that the identification of the genetic basis of AF will ultimately lead to the discovery of new pathways and therapeutic targets for this common arrhythmia. © 2007 Current Medicine Group LLC.
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页码:414 / 419
页数:5
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