A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome (Q33145572)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome |
scientific article |
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A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome (English)
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Krahn AD
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Wang J
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Spindler B
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Skanes AC
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Yee R
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Klein GJ
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Hegele RA
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1 July 2000
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140
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146-149
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