M. Brink

Long-term treated HIV infection is associated with platelet mitochondrial dysfunction

M. Jaeger, M. Netea, R. Rodenburg, 2021, Scientific Reports.

Major gradients in putatively nitrifying and non-nitrifying Archaea in the deep North Atlantic

J. Dinasquet, G. Herndl, H. Agogué, 2008, Nature.

Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency--a neurometabolic disorder associated with reduced L-serine biosynthesis.

R Berger, M. Durán, M. Pineda, 2000, American journal of human genetics.

Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy

Saskia B Wortmann, Rolph Pfundt, R. Pfundt, 2011, European Journal of Human Genetics.

NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect

R. Rodenburg, L. Nijtmans, F. Baertling, 2017, European Journal of Human Genetics.

A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13.

D. Misceo, R. Rodenburg, P. Strømme, 2016, European journal of medical genetics.

Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11.

T. Acker, R. Rodenburg, T. Haack, 2019, European journal of medical genetics.

Major gradients in putatively nitrifying and non-nitrifying Archaea in the deep North Atlantic

J. Dinasquet, G. Herndl, H. Agogué, 2009, Nature.