Mads G Stemmerik

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 2

Top Topics

Electron Transfer

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Mads G Stemmerik, Josefine de Stricker Borch, Morten Dunø, Thomas O Krag, John Vissing
Myopathy can be a key phenotype of membrin (GOSR2) deficiency. Human mutation 42 (9) (2021)
Daniel Raaschou-Pedersen, Karen L Madsen, Mads G Stemmerik, Anne-Sofie V Eisum, Volker Straub, John Vissing
Fat oxidation is impaired during exercise in lipin-1 deficiency. Neurology 93 (15) (2019)