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  1. 2019
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  8. 2018
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  16. 2017
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  28. 2016
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    Wilson, I. J., Carling, P. J., Alston, C. L., Floros, V. I., Pyle, A., Hudson, G., ... Chinnery, P. F. (2016). Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck. Human Molecular Genetics, 25(5), 1031-1041. https://doi.org/10.1093/hmg/ddv626
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  38. 2015
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    Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., ... Renieri, A. (2015). Evidence of digenic inheritance in Alport syndrome. Journal of Medical Genetics, 52(3), 163-174. https://doi.org/10.1136/jmedgenet-2014-102822
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    Sallevelt, S. C. E. H., Dreesen, J. C. F. M., De Coo, I. F. M., de Die-Smulders, C. E. M., & Smeets, H. J. M. (2015). Selecting the right embryo in mitochondrial disorders. In Screening the Single Euploid Embryo, Molecular Genetics in Reproductive Medicine (pp. 231). Springer.
  43. Published
    Körver-Keularts, I. M. L. W., de Visser, M., Bakker, H. D., Wanders, R. J. A., Vansenne, F., Scholte, H. R., ... van den Bosch, B. J. C. (2015). Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy. JIMD reports, 22, 39-45. https://doi.org/10.1007/8904_2015_409
  44. 2014
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  46. 2013
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    Rodenburg, R. J. T., Schoonderwoerd, G. C., Tiranti, V., Taylor, R. W., Roetig, A., Valente, L., ... van den Heuvel, L. P. (2013). A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disorders. Mitochondrion, 13(1), 36-43. https://doi.org/10.1016/j.mito.2012.11.004
  49. 2012
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  56. 2011
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    Bonneux, S., Fransen, E., Van Eyken, E., Van Laer, L., Huyghe, J., Van de Heyning, P., ... Van Camp, G. (2011). Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population. Mitochondrion, 11(5), 729-734. https://doi.org/10.1016/j.mito.2011.05.008
  59. Published
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