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List of works by Paulien Smits

Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs

scientific article

Functional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defects.

scientific article

Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies

scientific article

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

scientific article published on December 29, 2010

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