No Evidence for Association of SCO2 Heterozygosity with High-Grade Myopia or Other Diseases with Possible Mitochondrial DysfunctionDorota Piekutowska‐Abramczuk, Ewa Pronicka, Quan V. Hoang et al.|JIMD Reports|2015Cited by 8
The new molecular p.M177T identified in two unrelated patients with clinical features of SCO2-dependent cytochrome c oxidase deficiencyS. Brandon Luczak, Ewa Pronicka, Dorota Piekutowska‐Abramczuk et al.|Biochimica et Biophysica Acta (BBA) - Bioenergetics|2010Cited by 0
Detection of single large-scale mitochondrial DNA deletions by MLPA techniqueDorota Piekutowska‐Abramczuk, Ewa Pronicka, Anna Tańska et al.|Biochimica et Biophysica Acta (BBA) - Bioenergetics|2010Cited by 0
Molecular studies of Polish patients with respiratory chain complex I deficiencyPaweł Kowalski, Ewa Pronicka, Dorota Piekutowska‐Abramczuk et al.|Biochimica et Biophysica Acta (BBA) - Bioenergetics|2010Cited by 0