A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members. (September 2018)

• Record Type: Journal Article
• Authors: Dulovic, Marija; Schäffer, Eva; Leypoldt, Frank; Balck, Alexander; Schaake, Susen; Hinrichs, Frauke; Kirchner, Henriette; Brüggemann, Norbert; Berg, Daniela; Lohmann, Katja
• Is Part Of: Parkinsonism & related disorders. Volume 54(2018)
• Page Start: 116
• Page End: 118
• Publication Date: 2018-09
• Subjects: Neurogenetics -- Mitochondrial DNA mutation -- Genotype-driven treatment -- Klinefelter syndrome -- MERRF/Leigh-like syndrome; Parkinson's disease -- Periodicals; Movement disorders -- Periodicals; Movement Disorders -- Periodicals; Nerve Degeneration -- Periodicals; Nervous System Diseases -- Periodicals; Parkinson Disease -- Periodicals; Tremor -- Periodicals; Parkinson, Maladie de -- Périodiques; Parkinson's disease; 616.833
• DOI: 10.1016/j.parkreldis.2018.04.001
• Languages: English
• ISSNs: 1353-8020