Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants

Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants

Bibliographic Details
Main Authors: Göpel, Wolfgang, Berkowski, Sandra, Preuss, Michael, Ziegler, Andreas, Küster, Helmut, Felderhoff-Müser, Ursula, Gortner, Ludwig, Mögel, Michael, Härtel, Christoph, Herting, Egbert
Format: Online
Language:English
Published: BioMed Central 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236616/
id pubmed-4236616
recordtype oai_dc
spelling pubmed-42366162014-11-19 Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants Göpel, Wolfgang Berkowski, Sandra Preuss, Michael Ziegler, Andreas Küster, Helmut Felderhoff-Müser, Ursula Gortner, Ludwig Mögel, Michael Härtel, Christoph Herting, Egbert Research Article BioMed Central 2014-08-26 /pmc/articles/PMC4236616/ /pubmed/25155176 http://dx.doi.org/10.1186/1471-2431-14-210 Text en Copyright © 2014 Göpel et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Göpel, Wolfgang
Berkowski, Sandra
Preuss, Michael
Ziegler, Andreas
Küster, Helmut
Felderhoff-Müser, Ursula
Gortner, Ludwig
Mögel, Michael
Härtel, Christoph
Herting, Egbert
spellingShingle Göpel, Wolfgang
Berkowski, Sandra
Preuss, Michael
Ziegler, Andreas
Küster, Helmut
Felderhoff-Müser, Ursula
Gortner, Ludwig
Mögel, Michael
Härtel, Christoph
Herting, Egbert
Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
author_facet Göpel, Wolfgang
Berkowski, Sandra
Preuss, Michael
Ziegler, Andreas
Küster, Helmut
Felderhoff-Müser, Ursula
Gortner, Ludwig
Mögel, Michael
Härtel, Christoph
Herting, Egbert
author_sort Göpel, Wolfgang
title Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
title_short Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
title_full Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
title_fullStr Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
title_full_unstemmed Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
title_sort mitochondrial mutation m.1555a>g as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
description
publisher BioMed Central
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236616/
_version_ 1613158343054983168

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