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Matilainen, Sanna, Pirjo Isohanni, Liliya Euro, Tuula Lönnqvist, Helena Pihko, Tero Kivelä, Sakari Knuutila, and Anu Suomalainen. "Mitochondrial Encephalomyopathy and Retinoblastoma Explained By Compound Heterozygosity of SUCLA2 Point Mutation and 13q14 Deletion." Eur J Hum Genet 2017.

Matilainen, Sanna, et al. "Mitochondrial Encephalomyopathy and Retinoblastoma Explained By Compound Heterozygosity of SUCLA2 Point Mutation and 13q14 Deletion." Eur J Hum Genet 2017.