LQTS in Northern BC: homozygosity forKCNQ1V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function-Reference-Cited by-同舟云学术

LQTS in Northern BC: homozygosity forKCNQ1V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function

Published:2013-07-30 Issue:1 Volume:86 Page:85-90
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Jackson H.A.¹,McIntosh S.¹,Whittome B.¹,Asuri S.¹,Casey B.²,Kerr C.³,Tang A.³,Arbour L.T.¹

Affiliation:

1. Department of Medical Genetics and the Island Medical program; University of British Columbia; Victoria British Columbia Canada

2. Department of Pathology; Children's & Women's Health Centre; Vancouver British Columbia Canada

3. Department of Medicine, Division of Cardiology; University of British Columbia; Vancouver British Columbia Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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3. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death;Jervell;Am Heart J,1957

4. Long QT syndrome;Goldenberg;Curr Probl Cardiol,2008

5. Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel;Sanguinetti;Nature,1996

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