Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9

Tobias B. Haack, Florence Madignier, Martina Herzer, Eleonora Lamantea, Katharina Danhauser, Federica Invernizzi, Johannes Koch, Martin Freitag, Rene Drost, Ingo Hillier, Birgit Haberberger, Johannes A. Mayr, Uwe Ahting, Valeria Tiranti, Agnes Rötig, Arcangela Iuso, Rita Horvath, Marketa Tesarova, Ivo Baric, Graziella UzielBoris Rolinski, Wolfgang Sperl, Thomas Meitinger, Massimo Zeviani, Peter Freisinger, Holger Prokisch

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Medicine & Life Sciences