Mapping of a gene for long QT syndrome to chromosome 4q25-27.

Abstract : Long QT syndrome (LQTS) is a heterogeneous inherited disorder causing syncope and sudden death from ventricular arrhythmias. A first locus for this disorder was mapped to chromosome 11p15.5. However, locus heterogeneity has been demonstrated in several families, and two other loci have recently been located on chromosomes 7q35-36 and 3p21-24. We used linkage analysis to map the locus in a 65-member family in which LQTS was associated with more marked sinus bradycardia than usual, leading to sinus node dysfunction. Linkage to chromosome 11p15.5, 7q35-36, or 3p21-24 was excluded. Positive linkage was obtained for markers located on chromosome 4q25-27. A maximal LOD score of 7.05 was found for marker D4S402. The identification of a fourth locus for LQTS confirms its genetic heterogeneity. Locus 4q25-27 is associated with a peculiar phenotype within the LQTS entity.
Type de document :
Article dans une revue
American Journal of Human Genetics, Elsevier (Cell Press), 1995, 57 (5), pp.1114-22
Liste complète des métadonnées

https://hal-ensta.archives-ouvertes.fr/hal-01160657
Contributeur : Gilles Vergnaud <>
Soumis le : samedi 6 juin 2015 - 16:51:49
Dernière modification le : mardi 16 janvier 2018 - 15:33:13

Identifiants

Collections

Citation

J J Schott, F Charpentier, S Peltier, P Foley, E Drouin, et al.. Mapping of a gene for long QT syndrome to chromosome 4q25-27.. American Journal of Human Genetics, Elsevier (Cell Press), 1995, 57 (5), pp.1114-22. 〈hal-01160657〉

Partager

Métriques

Consultations de la notice

99