Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults-Reference-Cited by-同舟云学术

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults

Published:2015-07-17 Issue:32 Volume:37 Page:2552-2559
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:Eur Heart J

Author:

Ng Yi Shiau,Grady John P.,Lax Nichola Z.,Bourke John P.,Alston Charlotte L.,Hardy Steven A.,Falkous Gavin,Schaefer Andrew G.,Radunovic Aleksandar,Mohiddin Saidi A.,Ralph Matilda,Alhakim Ali,Taylor Robert W.,McFarland Robert,Turnbull Douglass M.,Gorman Gráinne S.

Funder

The Wellcome Trust

Newcastle University Centre for Ageing and Vitality

Biotechnology and Biological Sciences Research Council and Medical Research Council

Newcastle upon Tyne Hospitals NHS Foundation Trust, Lily Foundation and the UK NHS Specialist Commissioners

‘Rare Mitochondrial Disorders of Adults and Children’ Diagnostic Service in Newcastle upon Tyne

Newcastle NIHR Biomedical Research Centre, Newcastle and North Tyneside Comprehensive Local Research Network

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/37/32/2552/17357213/ehv306.pdf

Reference39 articles.

1. Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

2. Population prevalence of the MELAS A3243G mutation

3. Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

4. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease

5. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

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