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	1.	Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus. [electronic resource] by Soini, Heidi K Moilanen, Jukka S Finnila, Saara Majamaa, Kari Producer: 20130131 In: BMC research notes vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Adult-onset ataxia and polyneuropathy caused by mitochondrial 8993T-->C mutation. [electronic resource] by Rantamäki, Maria T Soini, Heidi K Finnilä, Saara M Majamaa, Kari Udd, Bjarne Producer: 20051031 In: Annals of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus. [electronic resource] by Soini, Heidi K Moilanen, Jukka S Vilmi-Kerälä, Tiina Finnilä, Saara Majamaa, Kari Producer: 20130826 In: BMC medical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mitochondrial hearing loss mutations among Finnish preterm and term-born infants. [electronic resource] by Soini, Heidi K Karjalainen, Minna K Hinttala, Reetta Rautio, Arja Hallman, Mikko Uusimaa, Johanna Publication details: Audiology research Jul 2017 In: Audiology research vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease. [electronic resource] by Soini, Heidi K Väisänen, Antti Kärppä, Mikko Hinttala, Reetta Kytövuori, Laura Moilanen, Jukka S Uusimaa, Johanna Majamaa, Kari Producer: 20170515 In: BMC medical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus. [electronic resource] by Uusimaa, Johanna Hinttala, Reetta Rantala, Heikki Päivärinta, Markku Herva, Riitta Röyttä, Matias Soini, Heidi Moilanen, Jukka S Remes, Anne M Hassinen, Ilmo E Majamaa, Kari Producer: 20080625 In: Epilepsia vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)