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

Crossref DOI link: https://doi.org/10.1186/1471-2431-14-210

Published: 2014-12

Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY

Authors

Göpel, Wolfgang

Berkowski, Sandra

Preuss, Michael

Ziegler, Andreas

Küster, Helmut

Felderhoff-Müser, Ursula

Gortner, Ludwig

Mögel, Michael

Härtel, Christoph

Herting, Egbert
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unspecified valid from 2014-08-26