Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease.

by Ekaterina Biterova, Alexander Ignatyev, Johanna Uusimaa, Reetta Hinttala, Lloyd W Ruddock
Published 2018-01-01

Mitochondrial hearing loss mutations among Finnish preterm and term-born infants

by Heidi K. Soini, Minna K. Karjalainen, Reetta Hinttala, Arja Rautio, Mikko Hallman, Johanna Uusimaa
Published 2017-11-01

Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder

by Laura Kytövuori, Mikko Kärppä, Hannu Tuominen, Johanna Uusimaa, Markku Saari, Reetta Hinttala, Kari Majamaa
Published 2017-05-01

Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCA disease

by Anniina E. Hiltunen, Salla M. Kangas, Steffen Ohlmeier, Ilkka Pietilä, Jori Hiltunen, Heikki Tanila, Colin McKerlie, Subashika Govindan, Hannu Tuominen, Riitta Kaarteenaho, Mikko Hallman, Johanna Uusimaa, Reetta Hinttala
Published 2020-12-01