Abstract:
BACKGROUND:Recombinant DNA technologies have facilitated the development of a set of polymorphic DNA markers covering the human genome. General linkage analysis in families predisposed to inherited disease is now feasible. Linkage analysis can help identify a disease gene even when relatively little is known about the disorder. METHODS AND RESULTS:Using this approach, we have identified linkage between a gene that causes the long QT syndrome and DNA markers on chromosome 11. CONCLUSIONS:The identification of the chromosomal location of the long QT locus is the first step in defining the specific mutations that cause this disease.
journal_name
Circulationjournal_title
Circulationauthors
Keating Mdoi
10.1161/01.cir.85.6.1973subject
Has Abstractpub_date
1992-06-01 00:00:00pages
1973-86issue
6eissn
0009-7322issn
1524-4539journal_volume
85pub_type
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