Literature DB >> 1350520

Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.

M Keating1.   

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.

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Year:  1992        PMID: 1350520     DOI: 10.1161/01.cir.85.6.1973

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  8 in total

1.  Evidence of a long QT founder gene with varying phenotypic expression in South African families.

Authors:  T de Jager; C H Corbett; J C Badenhorst; P A Brink; V A Corfield
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

Review 2.  Familial dilated cardiomyopathy.

Authors:  L Mestroni; M Krajinovic; G M Severini; B Pinamonti; A Di Lenarda; M Giacca; A Falaschi; F Camerini
Journal:  Br Heart J       Date:  1994-12

3.  Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349.

Authors:  M W Russell; M Dick; R M Campbell; J E Hulse; D J Munroe; E Bric; D E Housman; F S Collins; L C Brody
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

4.  Prenatal findings in patients with prolonged QT interval in the neonatal period.

Authors:  M Hofbeck; H Ulmer; E Beinder; E Sieber; H Singer
Journal:  Heart       Date:  1997-03       Impact factor: 5.994

Review 5.  Normal and abnormal consequences of apoptosis in the human heart: from postnatal morphogenesis to paroxysmal arrhythmias.

Authors:  T N James
Journal:  Trans Am Clin Climatol Assoc       Date:  1994

6.  A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

Authors:  A K Ewart; C A Morris; G J Ensing; J Loker; C Moore; M Leppert; M Keating
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

Review 7.  Translating genomic insights into cardiovascular medicine: Opportunities and challenges of CRISPR-Cas9.

Authors:  Yuan Zhang; Ioannis Karakikes
Journal:  Trends Cardiovasc Med       Date:  2020-06-27       Impact factor: 8.049

8.  Exploring mutation specific beta blocker pharmacology of the pathogenic late sodium channel current from patient-specific pluripotent stem cell myocytes derived from long QT syndrome mutation carriers.

Authors:  Thomas W Comollo; Xinle Zou; Chuangeng Zhang; Divya Kesters; Thomas Hof; Kevin J Sampson; Robert S Kass
Journal:  Channels (Austin)       Date:  2022-12       Impact factor: 3.493

  8 in total

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