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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Dades bibliogràfiques
Publicat a:	J Clin Invest
Autors principals:	Curran, M, Atkinson, D, Timothy, K, Vincent, G M, Moss, A J, Leppert, M, Keating, M
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1993
Matèries:	Research Article
Accés en línia:	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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