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JIMD Reports|May 6, 2015
Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel PhenotypesTuomas Komulainen, Milla-Riikka Hautakangas, Reetta Hinttala, et al.
Clinical Genetics|August 13, 2023
Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variantMilla-Riikka Hautakangas, Paula Widgren, Paavo Korpelainen, et al.
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