Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus

por Soini, Heidi K, Moilanen, Jukka S, Finnila, Saara, Majamaa, Kari
Publicado 2012

Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus

por Soini, Heidi K, Moilanen, Jukka S, Vilmi-Kerälä, Tiina, Finnilä, Saara, Majamaa, Kari
Publicado 2013

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

por Soini, Heidi K., Karjalainen, Minna K., Hinttala, Reetta, Rautio, Arja, Hallman, Mikko, Uusimaa, Johanna
Publicado 2017

A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease

por Soini, Heidi K., Väisänen, Antti, Kärppä, Mikko, Hinttala, Reetta, Kytövuori, Laura, Moilanen, Jukka S., Uusimaa, Johanna, Majamaa, Kari
Publicado 2017