MITOMAP References for Variant A-G at 9155

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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, 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 .