Literature DB >> 8316839

Evidence of genetic heterogeneity in the long QT syndrome.

J Benhorin, Y M Kalman, A Medina, J Towbin, N Rave-Harel, T D Dyer, J Blangero, J W MacCluer, B S Kerem.   

Abstract

Entities:  

Mesh：

Year:  1993        PMID： 8316839     DOI： 10.1126/science.8316839

Source DB:  PubMed          Journal:  Science        ISSN： 0036-8075            Impact factor:   47.728


× No keyword cloud information.
  9 in total

1.  Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.

Authors:  Liat Shushi; Batsheva Kerem; Maya Goldmit; Asher Peretz; Bernard Attali; Aron Medina; Jeffrey A Towbin; Junko Kurokawa; Robert S Kass; Jesaia Benhorin
Journal:  Ann Noninvasive Electrocardiol       Date:  2005-07       Impact factor: 1.468

2.  No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneity.

Authors:  Y L Ko; S A Chen; T K Tang; J L Lin; C E Chiang; J J Chen; M S Teng; M S Chang; W P Lien; C W Wu
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

3.  Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.

Authors:  L R Weitkamp; A J Moss; R A Lewis; W J Hall; J W MacCluer; P J Schwartz; E H Locati; D Tzivoni; G M Vincent; J L Robinson
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

4.  Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome.

Authors:  E Schulze-Bahr; W Haverkamp; H Wiebusch; H Schulte; M Hördt; M Borggrefe; G Breithardt; G Assmann; H Funke
Journal:  J Mol Med (Berl)       Date:  1995-11       Impact factor: 4.599

Review 5.  Molecular genetic aspects of the Romano-Ward long QT syndrome.

Authors:  J A Towbin
Journal:  Tex Heart Inst J       Date:  1994

6.  Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families.

Authors:  T Tanaka; K Nakahara; N Kato; T Imai; T Yamazaki; H Tomita; H Shimokawa; H Matsuhashi; N Sato; M Matsui
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

7.  Multiple endocrine neoplasia type 1 (MEN1) in two Asian families.

Authors:  B T Teh; S I Hii; R David; V Parameswaran; S Grimmond; M K Walters; T T Tan; D J Nancarrow; S P Chan; J Mennon
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

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

Authors:  J J Schott; F Charpentier; S Peltier; P Foley; E Drouin; J B Bouhour; P Donnelly; G Vergnaud; L Bachner; J P Moisan
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

9.  Calmodulin limits pathogenic Na+ channel persistent current.

Authors:  Haidun Yan; Chaojian Wang; Steven O Marx; Geoffrey S Pitt
Journal:  J Gen Physiol       Date:  2017-01-13       Impact factor: 4.086
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.