Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease (Q24290106)
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English | Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease |
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Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease (English)
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10 November 2000
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