Index | PMID | Date | Reference |
---|---|---|---|
1 | 27966441 | 2016 | Adema, A. Y., Janssen, M. C., van der Heijden, J. W. (2016) A novel mutation in mitochondrial DNA in a patient with diabetes, deafness and proteinuria The Netherlands Journal of Medicine . 74 (10): 455-457 . |
2 | 27450679 | 2017 | Sallevelt, S. C., de Die-Smulders, C. E., Hendrickx, A. T., Hellebrekers, D. M., de Coo, I. F., Alston, C. L., Knowles, C., Taylor, R. W., McFarland, R., Smeets, H. J. (2017) De novo mtDNA point mutations are common and have a low recurrence risk Journal of Medical Genetics . 54 (2): 73-83 . |
3 | NA | 2018 | Finsterer, J., Zarrouk-Mahjoub, S. (2018) Maternally inherited diabetes and deafness (MIDD) due to the m.9155A>G mutation, http://www.ijrsmhs.com/pdf/v3-i5/3.pdf International Journal of Research Studies in Medical and Health Sciences . 3 (5): 7-8 . |
4 | 34961688 | 2022 | Bergs, P. M. J., Maas, D. M., Janssen, M. C. H., Groothuis, J. T. (2022) Feasible and clinical relevant outcome measures for adults with mitochondrial disease Molecular and Cellular Biochemistry . 135 (1): 102-108 . |