Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system (Q40672037)
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scientific article published on February 2003
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English | Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system |
scientific article published on February 2003 |
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Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system (English)
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Arthur A M Wilde
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Connie R Bezzina
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Martin B Rook
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W Antoinette Groenewegen
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Lucas J Herfst
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Allard C van der Wal
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Jan Lam
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Habo J Jongsma
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Marcel M A M Mannens
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1 February 2003
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92
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2
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159-168
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Identifiers
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