Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block (Q33147836)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block |
scientific article |
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Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block (English)
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Lupoglazoff JM
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Denjoy I
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Cheav T
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Berthet M
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Extramiana F
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Cauchemez B
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Villain E
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Leenhardt A
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Guicheney P
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