Prevalence of mitochondrial 1555A → G mutation in European children

Maria Bitner-Glindzicz; Marcus Pembrey; Andrew Duncan; Jon Heron; Susan M. Ring; Amanda Hall; Shamima Rahman

doi:10.1056/NEJMc0806396

Prevalence of mitochondrial 1555A → G mutation in European children

Maria Bitner-Glindzicz
, Marcus Pembrey
, Andrew Duncan
, Jon Heron
, Susan M. Ring
, Amanda Hall
, Shamima Rahman

University College London
University of Bristol
MRC Centre for Neuromuscular Diseases, London

Research output: Contribution to journal › Letter, comment/opinion or interview › peer-review

143 Citations (Scopus)

81 Downloads (Pure)

Original language	English
Pages (from-to)	640-642
Number of pages	3
Journal	New England Journal of Medicine
Volume	360
Issue number	6
DOIs	https://doi.org/10.1056/NEJMc0806396
Publication status	Published - 5 Feb 2009

Bibliographical note

Keywords

aminoglycosides
anti-bacterial agents
audiometry
child
cost-benefit analysis
mitochondrial DNA
deafness
Europe
genetic testing
point mutation
prevalence

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10.1056/NEJMc0806396

Prevalence of Mitochondrial 1555A→G Mutation in European Children
Copyright © 2009 Massachusetts Medical Society. All rights reserved.
Final published version, 186 KB

Cite this

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title = "Prevalence of mitochondrial 1555A → G mutation in European children",

keywords = "aminoglycosides, anti-bacterial agents, audiometry, child, cost-benefit analysis, mitochondrial DNA, deafness, Europe, genetic testing, point mutation, prevalence",

author = "Maria Bitner-Glindzicz and Marcus Pembrey and Andrew Duncan and Jon Heron and Ring, \{Susan M.\} and Amanda Hall and Shamima Rahman",

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doi = "10.1056/NEJMc0806396",

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T1 - Prevalence of mitochondrial 1555A → G mutation in European children

AU - Bitner-Glindzicz, Maria

AU - Pembrey, Marcus

AU - Duncan, Andrew

AU - Heron, Jon

AU - Ring, Susan M.

AU - Hall, Amanda

AU - Rahman, Shamima

PY - 2009/2/5

Y1 - 2009/2/5

KW - aminoglycosides

KW - anti-bacterial agents

KW - audiometry

KW - child

KW - cost-benefit analysis

KW - mitochondrial DNA

KW - deafness

KW - Europe

KW - genetic testing

KW - point mutation

KW - prevalence

UR - http://www.nejm.org/doi/full/10.1056/NEJMc0806396

U2 - 10.1056/NEJMc0806396

DO - 10.1056/NEJMc0806396

M3 - Letter, comment/opinion or interview

C2 - 19196684

SN - 0028-4793

VL - 360

SP - 640

EP - 642

JO - New England Journal of Medicine

JF - New England Journal of Medicine

IS - 6

ER -

Prevalence of mitochondrial 1555A → G mutation in European children

Bibliographical note

Keywords

Access to Document

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Cite this