The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
収録刊行物
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- J Clin Invest
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J Clin Invest 118 2219-2229, 2008
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- CRID
- 1573105975597355392
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- NII論文ID
- 10030696440
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- データソース種別
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- CiNii Articles
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