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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Bibliografiset tiedot
Päätekijät: Curran, M, Atkinson, D, Timothy, K, Vincent, G M, Moss, A J, Leppert, M, Keating, M
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1993
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC294917/
https://ncbi.nlm.nih.gov/pubmed/8102381
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