Article
A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members.
Parkinsonism & related disorders - 1 Sept 2018
Dulovic Marija, Schäffer Eva, Leypoldt Frank, Balck Alexander, Schaake Susen, Hinrichs Frauke, Kirchner Henriette, Brüggemann Norbert, Berg Daniela, Lohmann Katja
Abstract excerpt
No abstract is available from the source.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.