Author(s): Rolfs, Prof. Arndt, MD, Klein, Prof. Christine, MD, Kandaswamy, Krishna Kumar, PhD, Lohmann, Katja, PhD, Brüggemann, Norbert, MD, Tadic, Vera, MD, Werber, Martin, Münchau, Alexander, MD, Dobricic, Valerija, PhD, Trinh, Joanne, Phd, Dulovic Mahlow, Marija, Nolte, Achim, Schäfer, Jochen, Imhoff, Sophie
A profound understanding of rare genetic disorders relies on the description of large numbers of patients. Based on its unique positioning in the rare disease field, CENTOGENE can significantly contribute on multiple levels. This is exemplified by a recent corresponding study in the Journal of Neurology.
A profound understanding of rare genetic disorders relies on the description of large numbers of patients. Based on its unique positioning in the rare disease field, CENTOGENE can significantly contribute on multiple levels. This is exemplified by a recent corresponding study in the Journal of Neurology.
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