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/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236616/

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