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...

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Bibliografske podrobnosti
izdano v:	J Clin Invest
Principais autores:	Curran, M, Atkinson, D, Timothy, K, Vincent, G M, Moss, A J, Leppert, M, Keating, M
Format:	Artigo
Jezik:	Inglês
Izdano:	American Society for Clinical Investigation 1993
Teme:	Research Article
Online dostop:	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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Locus heterogeneity of autosomal dominant long QT syndrome.

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