Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X. (Q50497138)
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scientific article published in April 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X. |
scientific article published in April 2000 |
Statements
Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X. (English)
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Wei J
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Fish FA
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Myerburg RJ
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Roden DM
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George AL Jr
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1 April 2000
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15
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4
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387-388
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