Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants (Q34538375)
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English | Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants |
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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 (English)
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Ursula Felderhoff-Müser
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Wolfgang Göpel
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Michael Mögel
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Egbert Herting
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Christoph Härtel
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German Neonatal Network
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Helmut Küster
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Sandra Berkowski
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Ludwig Gortner
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26 August 2014
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