Locus heterogeneity of autosomal dominant long QT syndrome.
Autosomal dominant long QT syndrome (LQT) is an inherited disorder that causes syncope and sudden death from cardiac arrhythmias. In genetic linkage studies of seven unrelated families we mapped a gene for LQT to the short arm of chromosome 11 (11p15.5), near the Harvey ras-1 gene (H ras-1). To dete...
שמור ב:
| הוצא לאור ב: | J Clin Invest |
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| Principais autores: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
1993
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC294917/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8102381/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116653 |
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