A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect
2006 ◽
Vol 43
(10)
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pp. 817-821
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2006 ◽
Vol 17
(5)
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pp. 480-485
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Keyword(s):
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2006 ◽
Vol 17
(3)
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pp. 270-275
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2010 ◽
Vol 52
(1)
◽
pp. e6-e8
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2006 ◽
Vol 17
(3)
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pp. 276-278
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