A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members

Article ID	Journal	Published Year	Pages	File Type
10227132	Parkinsonism & Related Disorders	2018	6 Pages	PDF

Keywords

Mitochondrial DNA mutation Klinefelter syndrome Neurogenetics

Related Topics

Life Sciences Biochemistry, Genetics and Molecular Biology Ageing

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A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members

Authors

Marija Dulovic, Eva Schäffer, Frank Leypoldt, Alexander Balck, Susen Schaake, Frauke Hinrichs, Henriette Kirchner, Norbert Brüggemann, Daniela Berg, Katja Lohmann,