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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書目詳細資料

發表在:	J Clin Invest
Principais autores:	Curran, M, Atkinson, D, Timothy, K, Vincent, G M, Moss, A J, Leppert, M, Keating, M
格式:	Artigo
語言:	Inglês
出版:	American Society for Clinical Investigation 1993
主題:	Research Article
在線閱讀:	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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