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Dive into the research topics of 'Mitochondrial Disease Caused by a Novel Homozygous Mutation (Gly106del) in the SCO1 Gene'. Together they form a unique fingerprint.- Sort by
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Ninna Brix, Janni Majgaard Jensen, Inge Søkilde Pedersen, Anja Ernst, Simon Frost, Pauline Bogaard, Michael B Petersen, Lars Bender
Research output: Contribution to journal › Journal article › Research › peer-review