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List of works by Fabian Baertling

Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration

scientific article

MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy

scientific article published on 24 March 2015

MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities

scientific article published on 10 February 2015

NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect.

scientific article

Neonatal encephalocardiomyopathy caused by mutations in VARS2.

scientific article

The many faces of paediatric mitochondrial disease on neuroimaging

scientific article

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