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Research Output 2019 2019

  • 1 Journal article

Mitochondrial Disease Caused by a Novel Homozygous Mutation (Gly106del) in the SCO1 Gene

Brix, N., Jensen, J. M., Pedersen, I. S., Ernst, A., Frost, S., Bogaard, P., Petersen, M. B. & Bender, L., Oct 2019, In : Neonatology. 116, 3, p. 290–294 5 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Mitochondrial Diseases
Muscle Hypotonia
Brain Diseases
Early Diagnosis