The E1784K mutation SCN5A is associated with mixed phenotype of type 3 long QT syndrome
Bibliographic Information
- Title
- The E1784K mutation SCN5A is associated with mixed phenotype of type 3 long QT syndrome
- Author
- Makita N, et. al.
Journal
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- J Clin Invest (印刷中)
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J Clin Invest (印刷中) 2008
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Details
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- CRID
- 1010000781983946114
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- Article Type
- journal article
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- Data Source
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- KAKEN