公開日期 | 題名 | 作者 | 關聯 | scopus | WOS | 全文 |
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2006 | A common SCN5A polymorphsim attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a chinese family with an inherited cardiac conduction defect | Niu, D. M.; Hwang, B.; Hwang, H. W.; Wang, N. H.; Wu, J. Y.; Lee, P. C.; Chien, J. C.; Shieh, R. C.; Chen, Y. T. | J Med Genet 43(10), 817-821 |