Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency
Johannes A. Mayr(Paracelsus Medical University), Wolfgang Sperl(Paracelsus Medical University), Florence Madignier(Helmholtz Zentrum München), Olaf A. Bodamer(Broad Institute), Franz Zimmermann(Paracelsus Medical University), Johannes Koch(Paracelsus Medical University), Tobias B. Haack(Technical University of Munich), Christian Rauscher(Paracelsus Medical University), Holger Prokisch(Helmholtz Zentrum München)
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