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
Göpel, Wolfgang
Berkowski, Sandra
Preuss, Michael
Ziegler, Andreas
Küster, Helmut
Felderhoff-Müser, Ursula
Gortner, Ludwig
Mögel, Michael
Härtel, Christoph
Herting, Egbert
unspecified valid from 2014-08-26